A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547719



Internal ID18499314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32137654..32584771hg38UCSC Ensembl
Innerchr15:32429855..32876972hg19UCSC Ensembl
Innerchr15:30217147..30664264hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38447118
hg19447118
hg18447118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039486
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)nssv3547719
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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