A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006676



Internal ID19095894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159194556..159226379hg38UCSC Ensembl
Innerchr2:160051067..160082890hg19UCSC Ensembl
Innerchr2:159759313..159791136hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3831824
hg1931824
hg1831824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582987
Samples
Known GenesTANC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006676
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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