A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997861



Internal ID18810711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158766425..158784871hg38UCSC Ensembl
Innerchr1:158736215..158754661hg19UCSC Ensembl
Innerchr1:157002839..157021285hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3818447
hg1918447
hg1818447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485649
Samples
Known GenesOR6N1, OR6N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997861
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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