A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523734



Internal ID15451027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28908779..28930485hg38UCSC Ensembl
Innerchr12:29061712..29083418hg19UCSC Ensembl
Innerchr12:28952979..28974685hg18UCSC Ensembl
Innerchr12:28952979..28974685hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3821707
hg1921707
hg1821707
hg1721707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699550
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523734
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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