A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639873



Internal ID6679963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7661216..7662812hg38UCSC Ensembl
Innerchr17:7661236..7662793hg38UCSC Ensembl
Outerchr17:7661197..7662832hg38UCSC Ensembl
chr17:7564534..7566130hg19UCSC Ensembl
Innerchr17:7564554..7566111hg19UCSC Ensembl
Outerchr17:7564515..7566150hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381597
hg191597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15604944, essv15604958, essv15604940, essv15604953, essv15604937, essv15604961, essv15604939, essv15604960, essv15604966, essv15604955, essv15604957, essv15604952, essv15604943, essv15604963, essv15604948, essv15604942, essv15604956, essv15604954, essv15604946, essv15604951, essv15604938, essv15604962, essv15604964, essv15604945, essv15604950, essv15604941, essv15604949, essv15604947, essv15604965, essv15604959, essv15604936
SamplesNA20508, NA19664, NA11995, HG01359, HG00257, NA12399, NA20806, HG03808, HG01766, NA20764, HG01124, HG00290, HG03785, HG00266, HG00145, HG02236, NA20809, NA12234, HG00373, HG03802, HG01182, HG03740, HG00140, HG02725, HG00246, HG04219, NA20902, NA20887, NA19818, HG01395, HG01086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639873
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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