A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15327843



Internal ID6844800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95775313..95786792hg38UCSC Ensembl
Innerchr15:95775463..95786642hg38UCSC Ensembl
Outerchr15:95775163..95786942hg38UCSC Ensembl
chr15:96318542..96330021hg19UCSC Ensembl
Innerchr15:96318692..96329871hg19UCSC Ensembl
Outerchr15:96318392..96330171hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3811480
hg1911480
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637341
Supporting Variants
SamplesNA20911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15327843
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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