A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711798



Internal ID15659068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25298555..25316105hg38UCSC Ensembl
Innerchr1:25625046..25642596hg19UCSC Ensembl
Innerchr1:25497633..25515183hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817551
hg1917551
hg1817551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545859
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)nssv711798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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