A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046074



Internal ID18788605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136228197..136393924hg38UCSC Ensembl
Innerchr9:139120043..139288376hg19UCSC Ensembl
Innerchr9:138259864..138408197hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38165728
hg19168334
hg18148334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759857
Samples
Known GenesCARD9, DKFZP434A062, DNLZ, GPSM1, QSOX2, SNAPC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046074
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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