A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635932



Internal ID7022729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25647036..25649837hg38UCSC Ensembl
Innerchr15:25647036..25649837hg38UCSC Ensembl
Outerchr15:25646927..25649843hg38UCSC Ensembl
chr15:25892183..25894984hg19UCSC Ensembl
Innerchr15:25892183..25894984hg19UCSC Ensembl
Outerchr15:25892074..25894990hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15188727, essv15188729, essv15188728
SamplesNA18749, NA18946, HG02116
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635932
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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