A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726012



Internal ID19024293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50274257..50354091hg38UCSC Ensembl
Innerchr2:50501395..50581229hg19UCSC Ensembl
Innerchr2:50354899..50434733hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3879835
hg1979835
hg1879835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000087
Supporting Variants
Samples
Known GenesNRXN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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