A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989287



Internal ID16283243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3425673..3428129hg38UCSC Ensembl
Innerchr4:3427400..3429856hg19UCSC Ensembl
Innerchr4:3397198..3399654hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg382457
hg192457
hg182457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593456
Supporting Variants
Samples
Known GenesRGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989287
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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