A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622752



Internal ID7009610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28641439..28648644hg38UCSC Ensembl
Innerchr10:28641439..28648644hg38UCSC Ensembl
Outerchr10:28640939..28649144hg38UCSC Ensembl
chr10:28930368..28937573hg19UCSC Ensembl
Innerchr10:28930368..28937573hg19UCSC Ensembl
Outerchr10:28929868..28938073hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg387206
hg197206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13738663, essv13738662
SamplesNA19434, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622752
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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