A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007563



Internal ID22069194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248585893..248661962hg38UCSC Ensembl
Outerchr1:248574146..248662519hg38UCSC Ensembl
Innerchr1:248749194..248825263hg19UCSC Ensembl
Outerchr1:248737447..248825820hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3888374
hg1988374
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155109
Supporting Variants
Samples
Known GenesOR2T10, OR2T11, OR2T27, OR2T34, OR2T35
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007563
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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