A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667259



Internal ID15057225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5267043..5335470hg38UCSC Ensembl
Innerchr9:5267043..5335470hg19UCSC Ensembl
Innerchr9:5257043..5325470hg18UCSC Ensembl
Innerchr9:5257043..5325470hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868428
hg1968428
hg1868428
hg1768428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516752
Supporting Variants
Samples
Known GenesRLN1, RLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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