A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526146



Internal ID15453439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29836359..29959890hg38UCSC Ensembl
Innerchr12:29989292..30112823hg19UCSC Ensembl
Innerchr12:29880559..30004090hg18UCSC Ensembl
Innerchr12:29880559..30004090hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38123532
hg19123532
hg18123532
hg17123532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702401
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526146
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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