A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15322544



Internal ID3095651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94251374..94257967hg38UCSC Ensembl
Innerchr15:94251874..94257467hg38UCSC Ensembl
Outerchr15:94250374..94258967hg38UCSC Ensembl
chr15:94794603..94801196hg19UCSC Ensembl
Innerchr15:94795103..94800696hg19UCSC Ensembl
Outerchr15:94793603..94802196hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386594
hg196594
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637309
Supporting Variants
SamplesHG02722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15322544
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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