A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019320



Internal ID19108538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11645592..11934134hg38UCSC Ensembl
Innerchr9:11645592..11934134hg19UCSC Ensembl
Innerchr9:11635592..11924134hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38288543
hg19288543
hg18288543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7412n100
Supporting Variantsnssv3689277
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)nsv1019320
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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