A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516637



Internal ID15097244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159919896..159938603hg38UCSC Ensembl
Innerchr1:159889686..159908393hg19UCSC Ensembl
Innerchr1:158156310..158175017hg18UCSC Ensembl
Innerchr1:156702759..156721466hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3818708
hg1918708
hg1818708
hg1718708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703037, nssv655349, nssv669784
Samples
Known GenesIGSF9, TAGLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516637
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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