A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704095



Internal ID3705911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15224045..15226296hg38UCSC Ensembl
Innerchr10:15224065..15226276hg38UCSC Ensembl
Outerchr10:15224025..15226316hg38UCSC Ensembl
chr10:15266044..15268295hg19UCSC Ensembl
Innerchr10:15266064..15268275hg19UCSC Ensembl
Outerchr10:15266024..15268315hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622441
Supporting Variants
SamplesNA19658
Known GenesFAM171A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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