A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035654



Internal ID19124873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112954828..113027616hg38UCSC Ensembl
Innerchr9:115717108..115789896hg19UCSC Ensembl
Innerchr9:114756929..114829717hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3872789
hg1972789
hg1872789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7703n100
Supporting Variantsnssv3695108
Samples
Known GenesZNF883
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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