A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545358



Internal ID16332767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9261182..9327252hg38UCSC Ensembl
Innerchr1:9321241..9387311hg19UCSC Ensembl
Innerchr1:9243828..9309898hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3866071
hg1966071
hg1866071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv96n54
Supporting Variantsnssv709664, nssv709665
Samples
Known GenesH6PD, SPSB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545358
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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