A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993114



Internal ID15940384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16518096..16555520hg38UCSC Ensembl
Innerchr4:16519719..16557143hg19UCSC Ensembl
Innerchr4:16128817..16166241hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3837425
hg1937425
hg1837425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593780
Supporting Variants
Samples
Known GenesLDB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv993114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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