A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256442



Internal ID1658792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56251223..56260386hg38UCSC Ensembl
Innerchr15:56251225..56260385hg38UCSC Ensembl
Outerchr15:56251222..56260388hg38UCSC Ensembl
chr15:56543421..56552584hg19UCSC Ensembl
Innerchr15:56543423..56552583hg19UCSC Ensembl
Outerchr15:56543420..56552586hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389164
hg199164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636581
Supporting Variants
SamplesHG01524
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256442
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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