A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690704



Internal ID18988985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20747782..20764240hg38UCSC Ensembl
Innerchr9:20747781..20764239hg19UCSC Ensembl
Innerchr9:20737781..20754239hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3816459
hg1916459
hg1816459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024327
Supporting Variants
Samples
Known GenesFOCAD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690704
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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