A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545840



Internal ID15986563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25338308hg38UCSC Ensembl
Innerchr1:25598276..25664799hg19UCSC Ensembl
Innerchr1:25470863..25537386hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3866524
hg1966524
hg1866524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv201n54
Supporting Variantsnssv711760, nssv711761, nssv711765, nssv711764, nssv711766, nssv711762, nssv711763
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545840
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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