A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009167



Internal ID19098385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:94662150..94833657hg38UCSC Ensembl
Innerchr2:95327875..95499402hg19UCSC Ensembl
Innerchr2:94691602..94863129hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38171508
hg19171528
hg18171528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729129
Samples
Known GenesANKRD20A8P, FAM95A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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