A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580079



Internal ID18878360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:98260587..98288031hg38UCSC Ensembl
Innerchr2:98877050..98904494hg19UCSC Ensembl
Innerchr2:98243482..98270926hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3827445
hg1927445
hg1827445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002366
Supporting Variants
Samples
Known GenesVWA3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580079
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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