A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044135



Internal ID18786666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116430237..116516729hg38UCSC Ensembl
Innerchr9:119192516..119279008hg19UCSC Ensembl
Innerchr9:118232337..118318829hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3886493
hg1986493
hg1886493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695167
Samples
Known GenesASTN2, LOC100128505
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044135
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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