A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715646



Internal ID19013927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24216571..24318270hg38UCSC Ensembl
Innerchr15:24461718..24563417hg19UCSC Ensembl
Innerchr15:22012811..22114510hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38101700
hg19101700
hg18101700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046909
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715646
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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