A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010061



Internal ID18752592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68554293..68655679hg38UCSC Ensembl
Innerchr4:69420011..69521397hg19UCSC Ensembl
Innerchr4:69102606..69203992hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38101387
hg19101387
hg18101387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5279n100
Supporting Variantsnssv3628738, nssv3628736, nssv3628737, nssv3628739
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)nsv1010061
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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