A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913046



Internal ID5084822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101251702..101252125hg38UCSC Ensembl
Innerchr10:101251706..101252121hg38UCSC Ensembl
Outerchr10:101251698..101252129hg38UCSC Ensembl
chr10:103011459..103011882hg19UCSC Ensembl
Innerchr10:103011463..103011878hg19UCSC Ensembl
Outerchr10:103011455..103011886hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624372
Supporting Variants
SamplesNA18546
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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