A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759791



Internal ID19058072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100715746..100747558hg38UCSC Ensembl
Innerchr9:103478028..103509840hg19UCSC Ensembl
Innerchr9:102517849..102549661hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3831813
hg1931813
hg1831813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036417
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)nssv3759791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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