A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522225



Internal ID15449518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728285..144177097hg38UCSC Ensembl
Innerchr7:143425378..143874190hg19UCSC Ensembl
Innerchr7:143056311..143505123hg18UCSC Ensembl
Innerchr7:142863026..143311838hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38448813
hg19448813
hg18448813
hg17448813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695002
Samples
Known GenesCTAGE6, FAM115A, FAM115C, LOC154761, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522225
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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