A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987664



Internal ID15934934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1165892..1421910hg38UCSC Ensembl
Innerchr4:1159680..1415698hg19UCSC Ensembl
Innerchr4:1149680..1405698hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38256019
hg19256019
hg18256019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593278
Supporting Variants
Samples
Known GenesCRIPAK, CTBP1, CTBP1-AS, CTBP1-AS2, LOC100130872, MAEA, SPON2, UVSSA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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