A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545833



Internal ID15986556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25300841hg38UCSC Ensembl
Innerchr1:25598276..25627332hg19UCSC Ensembl
Innerchr1:25470863..25499919hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3829057
hg1929057
hg1829057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv200n54
Supporting Variantsnssv711685, nssv711678, nssv711683, nssv711679, nssv711682, nssv711681, nssv711686, nssv711680, nssv711684
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545833
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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