A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545839



Internal ID15986562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25338175hg38UCSC Ensembl
Innerchr1:25598276..25664666hg19UCSC Ensembl
Innerchr1:25470863..25537253hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3866391
hg1966391
hg1866391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv201n54
Supporting Variantsnssv711752, nssv711753, nssv711747, nssv711759, nssv711756, nssv711743, nssv711745, nssv711749, nssv711757, nssv711741, nssv711751, nssv711755, nssv711746, nssv711758, nssv711750, nssv711748, nssv711742, nssv711744, nssv711754
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545839
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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