A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699866



Internal ID15089832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159916632..159953321hg38UCSC Ensembl
Innerchr1:159886422..159923111hg19UCSC Ensembl
Innerchr1:158153046..158189735hg18UCSC Ensembl
Innerchr1:156699495..156736184hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3836690
hg1936690
hg1836690
hg1736690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524006
Supporting Variants
Samples
Known GenesIGSF9, SLAMF9, TAGLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699866
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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