A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622491



Internal ID7009350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567393..17585156hg38UCSC Ensembl
Innerchr10:17567393..17585156hg38UCSC Ensembl
Outerchr10:17566893..17585656hg38UCSC Ensembl
chr10:17609392..17627155hg19UCSC Ensembl
Innerchr10:17609392..17627155hg19UCSC Ensembl
Outerchr10:17608892..17627655hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3817764
hg1917764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv99e214
Supporting Variantsessv13707112, essv13707113, essv13707111
SamplesHG01848, HG02512, HG02141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622491
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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