A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987689



Internal ID15934959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1344830..1420896hg38UCSC Ensembl
Innerchr4:1338618..1414684hg19UCSC Ensembl
Innerchr4:1328618..1404684hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876067
hg1976067
hg1876067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593302
Supporting Variants
Samples
Known GenesCRIPAK, UVSSA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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