A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998376



Internal ID18811226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159100546..159201276hg38UCSC Ensembl
Innerchr2:159957058..160057787hg19UCSC Ensembl
Innerchr2:159665304..159766033hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38100731
hg19100730
hg18100730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4096n100
Supporting Variantsnssv3582984
Samples
Known GenesMIR6888, TANC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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