A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13752229



Internal ID3754045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35196134..35198660hg38UCSC Ensembl
Innerchr10:35196182..35198612hg38UCSC Ensembl
Outerchr10:35196086..35198708hg38UCSC Ensembl
chr10:35485062..35487588hg19UCSC Ensembl
Innerchr10:35485110..35487540hg19UCSC Ensembl
Outerchr10:35485014..35487636hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382527
hg192527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622894
Supporting Variants
SamplesNA19448
Known GenesCREM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13752229
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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