A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528405



Internal ID15455698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:103502817..103507724hg38UCSC Ensembl
Innerchr12:103896595..103901502hg19UCSC Ensembl
Innerchr12:102420725..102425632hg18UCSC Ensembl
Innerchr12:102399062..102403969hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384908
hg194908
hg184908
hg174908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704997
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528405
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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