A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3484537



Internal ID18725492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248520087..248626379hg38UCSC Ensembl
Innerchr1:248683388..248789680hg19UCSC Ensembl
Innerchr1:246750011..246856303hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38106293
hg19106293
hg18106293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001321
Supporting Variants
Samples
Known GenesOR2G6, OR2T10, OR2T11, OR2T29, OR2T34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3484537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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