A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586181



Internal ID6626494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59380016..59380840hg38UCSC Ensembl
Innerchr1:59380066..59380790hg38UCSC Ensembl
Outerchr1:59379936..59380920hg38UCSC Ensembl
chr1:59845688..59846512hg19UCSC Ensembl
Innerchr1:59845738..59846462hg19UCSC Ensembl
Outerchr1:59845608..59846592hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9943015, essv9942944, essv9942951, essv9943006, essv9943014, essv9943008, essv9942980, essv9943001, essv9942961, essv9943007, essv9942983, essv9943009, essv9942997, essv9942957, essv9942976, essv9942978, essv9942969, essv9942977, essv9942999, essv9943000, essv9942993, essv9942958, essv9942982, essv9942952, essv9942949, essv9942945, essv9942965, essv9943012, essv9942966, essv9942994, essv9942989, essv9942959, essv9943002, essv9942955, essv9942988, essv9943013, essv9942992, essv9942972, essv9942946, essv9942973, essv9942948, essv9942981, essv9942990, essv9943018, essv9942947, essv9942964, essv9943020, essv9942985, essv9943017, essv9942991, essv9942970, essv9942971, essv9942986, essv9942963, essv9942967, essv9943003, essv9943019, essv9942954, essv9942996, essv9942974, essv9942984, essv9942975, essv9943010, essv9942962, essv9942960, essv9943004, essv9942950, essv9942968, essv9942956, essv9942995, essv9943005, essv9943016, essv9942979, essv9942953, essv9943011, essv9942998, essv9942987
SamplesHG02879, HG02580, NA19312, HG03354, NA18520, HG01130, NA18871, NA18933, HG03478, NA19209, NA18501, NA19149, HG02255, HG02450, HG02974, HG03212, HG02885, NA18865, NA19782, NA19834, HG02322, HG03401, HG03548, HG02973, NA20340, NA19043, NA19914, NA18934, HG03451, NA20356, HG02009, NA19443, NA19107, HG02772, HG02012, HG03436, HG03445, HG02851, HG03583, HG01136, HG01443, HG03085, NA19129, NA20291, HG03391, HG03397, NA18498, NA18522, HG02807, HG02429, HG02938, NA19159, NA18910, HG02479, HG02536, HG03297, HG03118, HG02881, HG02947, HG01095, NA20276, HG02629, HG02144, HG02561, HG03343, HG03025, HG03369, HG03449, HG02485, NA19171, NA19350, HG02555, HG01781, HG02051, NA19092, HG03095, NA19439
Known GenesFGGY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586181
Frequency
Sample Size2504
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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