A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271678



Internal ID5660813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65169617..65171412hg38UCSC Ensembl
Innerchr15:65169617..65171412hg38UCSC Ensembl
Outerchr15:65169505..65171561hg38UCSC Ensembl
chr15:65461955..65463750hg19UCSC Ensembl
Innerchr15:65461955..65463750hg19UCSC Ensembl
Outerchr15:65461843..65463899hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381796
hg191796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636750
Supporting Variants
SamplesNA19072
Known GenesCLPX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271678
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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