A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622763



Internal ID7009621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29011323..29017178hg38UCSC Ensembl
Innerchr10:29011356..29017145hg38UCSC Ensembl
Outerchr10:29011290..29017211hg38UCSC Ensembl
chr10:29300252..29306107hg19UCSC Ensembl
Innerchr10:29300285..29306074hg19UCSC Ensembl
Outerchr10:29300219..29306140hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385856
hg195856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13742666
SamplesHG00365
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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