A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545834



Internal ID15986557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25313871hg38UCSC Ensembl
Innerchr1:25598276..25640362hg19UCSC Ensembl
Innerchr1:25470863..25512949hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3842087
hg1942087
hg1842087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv203n54
Supporting Variantsnssv711693, nssv711687, nssv711695, nssv711694, nssv711697, nssv711691, nssv711698, nssv711699, nssv711688, nssv711696, nssv711690, nssv711692, nssv711689
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545834
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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