A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15270978



Internal ID1914160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63470912..63472776hg38UCSC Ensembl
Innerchr15:63470912..63472776hg38UCSC Ensembl
Outerchr15:63470735..63472891hg38UCSC Ensembl
chr15:63763111..63764975hg19UCSC Ensembl
Innerchr15:63763111..63764975hg19UCSC Ensembl
Outerchr15:63762934..63765090hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636717
Supporting Variants
SamplesHG01794
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15270978
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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