A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010352



Internal ID18752883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2431472..2480236hg38UCSC Ensembl
Innerchr4:2433199..2481963hg19UCSC Ensembl
Innerchr4:2402997..2451761hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3848765
hg1948765
hg1848765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616110
Samples
Known GenesLOC402160, RNF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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