A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999506



Internal ID19159043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34419042..34498124hg38UCSC Ensembl
Innerchr2:34644109..34723191hg19UCSC Ensembl
Innerchr2:34497613..34576695hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3879083
hg1979083
hg1879083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3757n100
Supporting Variantsnssv3728006
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)nsv999506
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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