A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704661



Internal ID15094627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:116569571..116596139hg38UCSC Ensembl
Innerchr12:117007376..117033944hg19UCSC Ensembl
Innerchr12:115491759..115518327hg18UCSC Ensembl
Innerchr12:115470096..115496664hg17UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3826569
hg1926569
hg1826569
hg1726569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528118
Supporting Variants
Samples
Known GenesMAP1LC3B2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704661
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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