A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545866



Internal ID15986589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25307714..25338175hg38UCSC Ensembl
Innerchr1:25634205..25664666hg19UCSC Ensembl
Innerchr1:25506792..25537253hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3830462
hg1930462
hg1830462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv209n54
Supporting Variantsnssv711846, nssv711842, nssv711847, nssv711845, nssv711844, nssv711843
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545866
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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