A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155107



Internal ID22085612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248585893..248647345hg38UCSC Ensembl
Outerchr1:248574146..248650779hg38UCSC Ensembl
Innerchr1:248749194..248810646hg19UCSC Ensembl
Outerchr1:248737447..248814080hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3876634
hg1976634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv27n97
Supporting Variantsnssv4007561
Samples
Known GenesOR2T10, OR2T11, OR2T27, OR2T34, OR2T35
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155107
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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