A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545864



Internal ID15986587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25307714..25329047hg38UCSC Ensembl
Innerchr1:25634205..25655538hg19UCSC Ensembl
Innerchr1:25506792..25528125hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3821334
hg1921334
hg1821334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n54
Supporting Variantsnssv711825, nssv711822, nssv711830, nssv711828, nssv711833, nssv711832, nssv711831, nssv711826, nssv711824, nssv711823, nssv711829, nssv711821, nssv711827, nssv711820
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545864
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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