A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006242



Internal ID16300198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:128060930..128061504hg38UCSC Ensembl
Innerchr4:128982085..128982659hg19UCSC Ensembl
Innerchr4:129201535..129202109hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38575
hg19575
hg18575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595389
Supporting Variants
Samples
Known GenesLARP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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