A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522992



Internal ID15450285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43614893..43618936hg38UCSC Ensembl
Innerchr10:44110341..44114384hg19UCSC Ensembl
Innerchr10:43430347..43434390hg18UCSC Ensembl
Innerchr10:43430347..43434390hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384044
hg194044
hg184044
hg174044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698662
Samples
Known GenesZNF485
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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