A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999954



Internal ID19159490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34460213..34512953hg38UCSC Ensembl
Innerchr2:34685280..34738020hg19UCSC Ensembl
Innerchr2:34538784..34591524hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3852741
hg1952741
hg1852741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n100
Supporting Variantsnssv3575130
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)nsv999954
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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