A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545161



Internal ID16332570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5043977..5110652hg38UCSC Ensembl
Innerchr1:5104037..5170712hg19UCSC Ensembl
Innerchr1:5003897..5070572hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3866676
hg1966676
hg1866676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n54
Supporting Variantsnssv708939, nssv708938
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545161
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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