A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002145



Internal ID16296101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569184..68624885hg38UCSC Ensembl
Innerchr4:69434902..69490603hg19UCSC Ensembl
Innerchr4:69117497..69173198hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3855702
hg1955702
hg1855702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594555
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)nssv1002145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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