A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029232



Internal ID19118451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11913048..12398327hg38UCSC Ensembl
Innerchr9:11913048..12398327hg19UCSC Ensembl
Innerchr9:11903048..12388327hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38485280
hg19485280
hg18485280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7426n100
Supporting Variantsnssv3758193
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)nsv1029232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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