A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527608



Internal ID15108215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76237926..76270397hg38UCSC Ensembl
Innerchr15:76530267..76562738hg19UCSC Ensembl
Innerchr15:74317322..74349793hg18UCSC Ensembl
Innerchr15:74317322..74349793hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3832472
hg1932472
hg1832472
hg1732472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704071
Samples
Known GenesETFA, TYRO3P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527608
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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