A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525630



Internal ID15452923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79051982..79066968hg38UCSC Ensembl
Innerchr15:79344324..79359310hg19UCSC Ensembl
Innerchr15:77131379..77146365hg18UCSC Ensembl
Innerchr15:77131379..77146365hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3814987
hg1914987
hg1814987
hg1714987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701783
Samples
Known GenesRASGRF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525630
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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