A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15338612



Internal ID6552066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98356826..98357403hg38UCSC Ensembl
Innerchr15:98356827..98357402hg38UCSC Ensembl
Outerchr15:98356825..98357404hg38UCSC Ensembl
chr15:98900055..98900632hg19UCSC Ensembl
Innerchr15:98900056..98900631hg19UCSC Ensembl
Outerchr15:98900054..98900633hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637405
Supporting Variants
SamplesNA20753
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15338612
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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