A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690615



Internal ID18642210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13764919..14226169hg38UCSC Ensembl
Innerchr9:13764918..14226168hg19UCSC Ensembl
Innerchr9:13754918..14216168hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38461251
hg19461251
hg18461251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033764
Supporting Variants
Samples
Known GenesLINC00583, NFIB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690615
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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