A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545836



Internal ID15986559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25320442hg38UCSC Ensembl
Innerchr1:25598276..25646933hg19UCSC Ensembl
Innerchr1:25470863..25519520hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3848658
hg1948658
hg1848658
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv204n54
Supporting Variantsnssv711712, nssv711705, nssv711713, nssv711707, nssv711708, nssv711711, nssv711706, nssv711709, nssv711710
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545836
Frequency
Sample Size17421
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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