A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153425



Internal ID15879459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:337951..480163hg38UCSC Ensembl
Innerchr4:331740..473952hg19UCSC Ensembl
Innerchr4:321740..463952hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38142213
hg19142213
hg18142213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593199
Supporting Variants
SamplesHGDP01369
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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