A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661872



Internal ID15051838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:11305872..11312762hg38UCSC Ensembl
Innerchr12:11458806..11465696hg19UCSC Ensembl
Innerchr12:11350073..11356963hg18UCSC Ensembl
Innerchr12:11350073..11356963hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg386891
hg196891
hg186891
hg176891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516262
Supporting Variants
Samples
Known GenesPRB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661872
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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