A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545837



Internal ID15986560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25329047hg38UCSC Ensembl
Innerchr1:25598276..25655538hg19UCSC Ensembl
Innerchr1:25470863..25528125hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3857263
hg1957263
hg1857263
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv204n54
Supporting Variantsnssv711729, nssv711727, nssv711717, nssv711723, nssv711728, nssv711718, nssv711722, nssv711715, nssv711720, nssv711724, nssv711714, nssv711716, nssv711726, nssv711719, nssv711725, nssv711721
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545837
Frequency
Sample Size17421
Observed Gain1
Observed Loss15
Observed Complex0
Frequencyn/a


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