A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3483532



Internal ID18724487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248589903..248645796hg38UCSC Ensembl
Innerchr1:248753204..248809097hg19UCSC Ensembl
Innerchr1:246819827..246875720hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3855894
hg1955894
hg1855894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003216
Supporting Variants
Samples
Known GenesOR2T10, OR2T11, OR2T35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3483532
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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