A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697596



Internal ID18649191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102880999..103100894hg38UCSC Ensembl
Innerchr9:105643281..105863176hg19UCSC Ensembl
Innerchr9:104683102..104902997hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38219896
hg19219896
hg18219896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051059
Supporting Variants
Samples
Known GenesCYLC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697596
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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