A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529049



Internal ID15109656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:93841701..93842109hg38UCSC Ensembl
Innerchr12:94235477..94235885hg19UCSC Ensembl
Innerchr12:92759608..92760016hg18UCSC Ensembl
Innerchr12:92737945..92738353hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38409
hg19409
hg18409
hg17409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705769
Samples
Known GenesCRADD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529049
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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