A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050777



Internal ID19139996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84443287..84559247hg38UCSC Ensembl
Innerchr9:87058202..87174162hg19UCSC Ensembl
Innerchr9:86248022..86363982hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38115961
hg19115961
hg18115961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7686n100
Supporting Variantsnssv3697531
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)nsv1050777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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