A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054932



Internal ID19144151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102823385..102884147hg38UCSC Ensembl
Innerchr9:105585667..105646429hg19UCSC Ensembl
Innerchr9:104625488..104686250hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860763
hg1960763
hg1860763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697595
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)nsv1054932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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