A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935578



Internal ID2506111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111156016..111242802hg38UCSC Ensembl
Innerchr10:111156516..111242302hg38UCSC Ensembl
Outerchr10:111155016..111243802hg38UCSC Ensembl
chr10:112915774..113002560hg19UCSC Ensembl
Innerchr10:112916274..113002060hg19UCSC Ensembl
Outerchr10:112914774..113003560hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3886787
hg1986787
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624549
Supporting Variants
SamplesHG02224
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935578
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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