A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545863



Internal ID15986586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25307714..25320442hg38UCSC Ensembl
Innerchr1:25634205..25646933hg19UCSC Ensembl
Innerchr1:25506792..25519520hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812729
hg1912729
hg1812729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711811, nssv711817, nssv711807, nssv711812, nssv711806, nssv711803, nssv711816, nssv711804, nssv711815, nssv711813, nssv711809, nssv711808, nssv711818, nssv711805, nssv711814, nssv711819, nssv711810
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545863
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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