A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622091



Internal ID7008950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:952113..979899hg38UCSC Ensembl
Innerchr10:952113..979899hg38UCSC Ensembl
Outerchr10:951942..980007hg38UCSC Ensembl
chr10:998053..1025839hg19UCSC Ensembl
Innerchr10:998053..1025839hg19UCSC Ensembl
Outerchr10:997882..1025947hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3827787
hg1927787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv89e214
Supporting Variantsessv13664660, essv13664661, essv13664662, essv13664659
SamplesNA19921, HG02568, NA19435, HG03470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622091
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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