A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526914



Internal ID15454207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115200985..115204518hg38UCSC Ensembl
Innerchr12:115638790..115642323hg19UCSC Ensembl
Innerchr12:114123173..114126706hg18UCSC Ensembl
Innerchr12:114101510..114105043hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg383534
hg193534
hg183534
hg173534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703275
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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