A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033764



Internal ID18776297
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 StatusM
Merged Variants
Supporting Variantsnssv3690615
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)nsv1033764
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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