A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007548



Internal ID22069179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248585893..248633912hg38UCSC Ensembl
Outerchr1:248574146..248645256hg38UCSC Ensembl
Innerchr1:248749194..248797213hg19UCSC Ensembl
Outerchr1:248737447..248808557hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3871111
hg1971111
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155106
Supporting Variants
Samples
Known GenesOR2T10, OR2T11, OR2T34, OR2T35
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007548
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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