A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040477



Internal ID19129696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112954828..113006489hg38UCSC Ensembl
Innerchr9:115717108..115768769hg19UCSC Ensembl
Innerchr9:114756929..114808590hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851662
hg1951662
hg1851662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7703n100
Supporting Variantsnssv3759805
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)nsv1040477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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