A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998268



Internal ID19157805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68509225..68674295hg38UCSC Ensembl
Innerchr4:69374943..69540013hg19UCSC Ensembl
Innerchr4:69057538..69222608hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38165071
hg19165071
hg18165071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5269n100
Supporting Variantsnssv3629549
Samples
Known GenesUGT2B15, UGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998268
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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