A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637002



Internal ID7023796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79672455..79679916hg38UCSC Ensembl
Innerchr15:79672466..79679905hg38UCSC Ensembl
Outerchr15:79672444..79679927hg38UCSC Ensembl
chr15:79964797..79972258hg19UCSC Ensembl
Innerchr15:79964808..79972247hg19UCSC Ensembl
Outerchr15:79964786..79972269hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387462
hg197462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15304686, essv15304685
SamplesNA19003, NA18941
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637002
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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