A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6318758



Internal ID9527203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80772640..80776605hg38UCSC Ensembl
Outerchr15:80772483..80776758hg38UCSC Ensembl
Innerchr15:81064981..81068946hg19UCSC Ensembl
Outerchr15:81064824..81069099hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384276
hg194276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658056
Supporting Variants
SamplesNA19056
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6318758
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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