A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636992



Internal ID7023786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78864016..78864627hg38UCSC Ensembl
Innerchr15:78864066..78864577hg38UCSC Ensembl
Outerchr15:78863905..78864738hg38UCSC Ensembl
chr15:79156358..79156969hg19UCSC Ensembl
Innerchr15:79156408..79156919hg19UCSC Ensembl
Outerchr15:79156247..79157080hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15302317, essv15302318, essv15302319
SamplesNA12777, HG01161, HG03598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636992
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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