A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045079



Internal ID19134298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105175758..105213314hg38UCSC Ensembl
Innerchr9:107938039..107975595hg19UCSC Ensembl
Innerchr9:106977860..107015416hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3837557
hg1937557
hg1837557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697638
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)nsv1045079
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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