A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15312209



Internal ID3670902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83226931..83236300hg38UCSC Ensembl
Innerchr15:83226933..83236298hg38UCSC Ensembl
Outerchr15:83226929..83236302hg38UCSC Ensembl
chr15:83895683..83905052hg19UCSC Ensembl
Innerchr15:83895685..83905050hg19UCSC Ensembl
Outerchr15:83895681..83905054hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg389370
hg199370
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637068
Supporting Variants
SamplesHG03270
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15312209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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