A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032861



Internal ID19122083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15378194..15410431hg38UCSC Ensembl
Innerchr9:15378192..15410429hg19UCSC Ensembl
Innerchr9:15368192..15400429hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3832238
hg1932238
hg1832238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7460n100
Supporting Variantsnssv3690625
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)nsv1032861
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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