A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528098



Internal ID15455391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97641041..97644081hg38UCSC Ensembl
Innerchr14:98107378..98110418hg19UCSC Ensembl
Innerchr14:97177131..97180171hg18UCSC Ensembl
Innerchr14:97177131..97180171hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383041
hg193041
hg183041
hg173041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704638
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528098
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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