A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023172



Internal ID19112389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11600297..11802691hg38UCSC Ensembl
Innerchr9:11600297..11802691hg19UCSC Ensembl
Innerchr9:11590297..11792691hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38202395
hg19202395
hg18202395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7413n100
Supporting Variantsnssv3689241
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)nsv1023172
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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