A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711681



Internal ID15658951
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 StatusS
Merged Variantsnsv545833
Supporting Variants
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711681
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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