A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv908360



Internal ID16202316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50023620..50047636hg38UCSC Ensembl
Innerchr2:50250758..50274774hg19UCSC Ensembl
Innerchr2:50104262..50128278hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3824017
hg1924017
hg1824017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581838
Supporting Variants
Samples
Known GenesNRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv908360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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