A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545629



Internal ID16333038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16013965..16054087hg38UCSC Ensembl
Innerchr1:16340460..16380582hg19UCSC Ensembl
Innerchr1:16213047..16253169hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3840123
hg1940123
hg1840123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155n54
Supporting Variantsnssv1173780
SamplesHGDP01090
Known GenesCLCNKA, CLCNKB, HSPB7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545629
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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