A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636347



Internal ID7023141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45768194..45970343hg38UCSC Ensembl
Innerchr15:45768214..45970324hg38UCSC Ensembl
Outerchr15:45768175..45970363hg38UCSC Ensembl
chr15:46060392..46262541hg19UCSC Ensembl
Innerchr15:46060412..46262522hg19UCSC Ensembl
Outerchr15:46060373..46262561hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38202150
hg19202150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15236001, essv15236000
SamplesHG03629, HG03733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636347
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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