A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043600



Internal ID19132819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54618395..54717958hg38UCSC Ensembl
Innerchr15:54910593..55010156hg19UCSC Ensembl
Innerchr15:52697885..52797448hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3899564
hg1999564
hg1899564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716732
Samples
Known GenesUNC13C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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