A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006916



Internal ID15954186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133948569..134042224hg38UCSC Ensembl
Innerchr4:134869724..134963379hg19UCSC Ensembl
Innerchr4:135089174..135182829hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3893656
hg1993656
hg1893656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595471
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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