A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656916



Internal ID15046882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19210244..19408609hg38UCSC Ensembl
Innerchr12:19363178..19561543hg19UCSC Ensembl
Innerchr12:19254445..19452810hg18UCSC Ensembl
Innerchr12:19254445..19452810hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38198366
hg19198366
hg18198366
hg17198366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516362
Supporting Variants
Samples
Known GenesPLEKHA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656916
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer