A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526485



Internal ID15453778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:59019021..59028887hg38UCSC Ensembl
Innerchr12:59412802..59422668hg19UCSC Ensembl
Innerchr12:57699069..57708935hg18UCSC Ensembl
Innerchr12:57699069..57708935hg17UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg389867
hg199867
hg189867
hg179867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702794
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526485
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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