A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527527



Internal ID15108134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197842688..198087104hg38UCSC Ensembl
Innerchr3:197569559..197813975hg19UCSC Ensembl
Innerchr3:199053956..199298372hg18UCSC Ensembl
Innerchr3:199057869..199302285hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38244417
hg19244417
hg18244417
hg17244417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703984
Samples
Known GenesANKRD18DP, IQCG, LMLN, LRCH3, RPL35A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527527
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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