A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv925151



Internal ID15872421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165156121..165159737hg38UCSC Ensembl
Innerchr2:166012631..166016247hg19UCSC Ensembl
Innerchr2:165720877..165724493hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383617
hg193617
hg183617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583563
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)nssv925151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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