A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697067



Internal ID15087033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98262605..98330034hg38UCSC Ensembl
Innerchr9:101024887..101092316hg19UCSC Ensembl
Innerchr9:100064708..100132137hg18UCSC Ensembl
Innerchr9:98104442..98171871hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3867430
hg1967430
hg1867430
hg1767430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519818
Supporting Variants
Samples
Known GenesGABBR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697067
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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