A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622067



Internal ID7008926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73560..74551hg38UCSC Ensembl
Innerchr10:73583..74528hg38UCSC Ensembl
Outerchr10:73537..74574hg38UCSC Ensembl
chr10:119500..120491hg19UCSC Ensembl
Innerchr10:119523..120468hg19UCSC Ensembl
Outerchr10:119477..120514hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13664117, essv13664088, essv13664078, essv13664090, essv13664085, essv13664091, essv13664122, essv13664130, essv13664135, essv13664123, essv13664137, essv13664112, essv13664108, essv13664086, essv13664083, essv13664142, essv13664100, essv13664131, essv13664111, essv13664095, essv13664129, essv13664141, essv13664089, essv13664103, essv13664115, essv13664133, essv13664136, essv13664104, essv13664118, essv13664114, essv13664126, essv13664099, essv13664094, essv13664106, essv13664121, essv13664116, essv13664084, essv13664120, essv13664102, essv13664097, essv13664134, essv13664132, essv13664128, essv13664138, essv13664105, essv13664093, essv13664076, essv13664081, essv13664119, essv13664127, essv13664096, essv13664113, essv13664082, essv13664107, essv13664124, essv13664110, essv13664140, essv13664087, essv13664079, essv13664098, essv13664080, essv13664101, essv13664139, essv13664092, essv13664077, essv13664109, essv13664125
SamplesHG01413, HG01173, HG01098, HG01052, HG01537, NA20531, NA18979, HG03589, NA20752, HG00640, NA19795, HG01305, HG02691, NA12400, NA20771, HG03950, HG00109, NA20768, HG03629, HG00369, NA20513, HG01668, HG00281, HG02597, HG01757, NA12044, HG01308, HG04047, HG01164, HG00349, NA12777, NA19707, HG01612, NA18939, NA20832, HG02497, HG01049, NA20581, HG02283, NA19752, NA19761, HG03006, HG01697, HG02722, NA20773, HG00383, HG00353, HG03899, HG00734, HG00136, HG01174, NA20516, NA07037, HG03733, HG02032, NA19713, HG00123, NA12830, HG00343, NA20528, HG01105, HG01775, HG03931, NA20908, HG01061, NA12776, NA18620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622067
Frequency
Sample Size2504
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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