A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547730



Internal ID18846011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32363158hg38UCSC Ensembl
Innerchr15:32458661..32655359hg19UCSC Ensembl
Innerchr15:30245953..30442651hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38196699
hg19196699
hg18196699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053539
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547730
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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