A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997456



Internal ID19156992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34460213..34512096hg38UCSC Ensembl
Innerchr2:34685280..34737163hg19UCSC Ensembl
Innerchr2:34538784..34590667hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3851884
hg1951884
hg1851884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n100
Supporting Variantsnssv3575129, nssv3575126, nssv3575127, nssv3575128
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997456
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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