A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997486



Internal ID18810336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:19965210..20072497hg38UCSC Ensembl
Innerchr3:20006702..20113989hg19UCSC Ensembl
Innerchr3:19981706..20088993hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38107288
hg19107288
hg18107288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593099
Samples
Known GenesKAT2B, PP2D1, RAB5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997486
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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