A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728084



Internal ID19026365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34460213..34515960hg38UCSC Ensembl
Innerchr2:34685280..34741027hg19UCSC Ensembl
Innerchr2:34538784..34594531hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3855748
hg1955748
hg1855748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004770
Supporting Variants
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)nssv3728084
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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