A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050853



Internal ID19140072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84447073..84559247hg38UCSC Ensembl
Innerchr9:87061988..87174162hg19UCSC Ensembl
Innerchr9:86251808..86363982hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38112175
hg19112175
hg18112175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7686n100
Supporting Variantsnssv3697532
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)nsv1050853
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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