A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023275



Internal ID19112492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10681431..11191502hg38UCSC Ensembl
Innerchr9:10681431..11191502hg19UCSC Ensembl
Innerchr9:10671431..11181502hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38510072
hg19510072
hg18510072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758165
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)nsv1023275
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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