A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635929



Internal ID7022726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25561307..25563713hg38UCSC Ensembl
Innerchr15:25561317..25563703hg38UCSC Ensembl
Outerchr15:25561297..25563723hg38UCSC Ensembl
chr15:25806454..25808860hg19UCSC Ensembl
Innerchr15:25806464..25808850hg19UCSC Ensembl
Outerchr15:25806444..25808870hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15188707
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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