A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759803



Internal ID18711398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111940569..111977059hg38UCSC Ensembl
Innerchr9:114702849..114739339hg19UCSC Ensembl
Innerchr9:113742670..113779160hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3836491
hg1936491
hg1836491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035481
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759803
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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