A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015379



Internal ID19104596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11582831..11869609hg38UCSC Ensembl
Innerchr9:11582831..11869609hg19UCSC Ensembl
Innerchr9:11572831..11859609hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38286779
hg19286779
hg18286779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7412n100
Supporting Variantsnssv3758171
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)nsv1015379
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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