A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547735



Internal ID18499330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32565199hg38UCSC Ensembl
Innerchr15:32458661..32857400hg19UCSC Ensembl
Innerchr15:30245953..30644692hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38398740
hg19398740
hg18398740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048688
Supporting Variants
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, 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)nssv3547735
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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