A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695702



Internal ID15085668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103016508..103065533hg38UCSC Ensembl
Innerchr9:105778790..105827815hg19UCSC Ensembl
Innerchr9:104818611..104867636hg18UCSC Ensembl
Innerchr9:102858345..102907370hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3849026
hg1949026
hg1849026
hg1749026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516844
Supporting Variants
Samples
Known GenesCYLC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695702
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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