A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581659



Internal ID18879940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50023197..50046929hg38UCSC Ensembl
Innerchr2:50250335..50274067hg19UCSC Ensembl
Innerchr2:50103839..50127571hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3823733
hg1923733
hg1823733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004550
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)nssv3581659
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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