A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701940



Internal ID15438592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38524632..38792755hg38UCSC Ensembl
Innerchr15:38816833..39084956hg19UCSC Ensembl
Innerchr15:36604125..36872248hg18UCSC Ensembl
Innerchr15:36604125..36872248hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38268124
hg19268124
hg18268124
hg17268124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525770
Supporting Variants
Samples
Known GenesC15orf53, RASGRP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701940
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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