A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv925186



Internal ID15872456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165158204..165159577hg38UCSC Ensembl
Innerchr2:166014714..166016087hg19UCSC Ensembl
Innerchr2:165722960..165724333hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381374
hg191374
hg181374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583570
Supporting Variants
Samples
Known GenesSCN3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv925186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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