A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13696308



Internal ID1443733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12272276..12310586hg38UCSC Ensembl
Innerchr10:12272327..12310535hg38UCSC Ensembl
Outerchr10:12272225..12310637hg38UCSC Ensembl
chr10:12314275..12352585hg19UCSC Ensembl
Innerchr10:12314326..12352534hg19UCSC Ensembl
Outerchr10:12314224..12352636hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3838311
hg1938311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622366
Supporting Variants
SamplesHG01334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13696308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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