A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987407



Internal ID16281363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:359166..440290hg38UCSC Ensembl
Innerchr4:352955..434079hg19UCSC Ensembl
Innerchr4:342955..424079hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3881125
hg1981125
hg1881125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593201
Supporting Variants
Samples
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987407
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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