A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689239



Internal ID18987520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11596157..11623397hg38UCSC Ensembl
Innerchr9:11596157..11623397hg19UCSC Ensembl
Innerchr9:11586157..11613397hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3827241
hg1927241
hg1827241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034601
Supporting Variants
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)nssv3689239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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