A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039638



Internal ID18782169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:67899571..68006091hg38UCSC Ensembl
Innerchr12:68293351..68399871hg19UCSC Ensembl
Innerchr12:66579618..66686138hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38106521
hg19106521
hg18106521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524603
Samples
Known GenesIFNG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039638
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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