A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547779



Internal ID18499374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32637651hg38UCSC Ensembl
Innerchr15:32458661..32929852hg19UCSC Ensembl
Innerchr15:30245953..30717144hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38471192
hg19471192
hg18471192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046929
Supporting Variants
Samples
Known GenesARHGAP11A, CHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547779
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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