A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005195



Internal ID18747726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159482969..159940547hg38UCSC Ensembl
Innerchr1:159452759..159910337hg19UCSC Ensembl
Innerchr1:157719383..158176961hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38457579
hg19457579
hg18457579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3490007
Samples
Known GenesAPCS, C1orf204, CCDC19, CRP, DUSP23, FCRL6, IGSF9, OR10J5, SLAMF8, TAGLN2, VSIG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005195
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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