A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13742665



Internal ID6014885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29001592..29004629hg38UCSC Ensembl
Innerchr10:29001648..29004573hg38UCSC Ensembl
Outerchr10:29001536..29004685hg38UCSC Ensembl
chr10:29290521..29293558hg19UCSC Ensembl
Innerchr10:29290577..29293502hg19UCSC Ensembl
Outerchr10:29290465..29293614hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622762
Supporting Variants
SamplesNA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13742665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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