A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052657



Internal ID19141876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122565623..122577487hg38UCSC Ensembl
Innerchr9:125327902..125339766hg19UCSC Ensembl
Innerchr9:124367723..124379587hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3811865
hg1911865
hg1811865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695227
Samples
Known GenesOR1L8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052657
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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