A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616111



Internal ID18567706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2962353..3017315hg38UCSC Ensembl
Innerchr4:2964080..3019042hg19UCSC Ensembl
Innerchr4:2933878..2988840hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3854963
hg1954963
hg1854963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008781
Supporting Variants
Samples
Known GenesGRK4, NOP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616111
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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