A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527889



Internal ID15108496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86866726..87203287hg38UCSC Ensembl
Innerchr7:86496042..86832603hg19UCSC Ensembl
Innerchr7:86333978..86670539hg18UCSC Ensembl
Innerchr7:86140693..86477254hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38336562
hg19336562
hg18336562
hg17336562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704392
Samples
Known GenesDMTF1, KIAA1324L, TMEM243
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527889
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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