A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593986



Internal ID16381395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36542165..36598599hg38UCSC Ensembl
Innerchr4:36543787..36600221hg19UCSC Ensembl
Innerchr4:36220182..36276616hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3856435
hg1956435
hg1856435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9010n54
Supporting Variantsnssv995861, nssv995862
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593986
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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