A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018488



Internal ID18761021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38021455..38455960hg38UCSC Ensembl
Innerchr9:38021452..38455957hg19UCSC Ensembl
Innerchr9:38011452..38445957hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38434506
hg19434506
hg18434506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688890
Samples
Known GenesALDH1B1, IGFBPL1, SHB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018488
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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