A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154439



Internal ID22084944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184646248..184714357hg38UCSC Ensembl
Outerchr1:184640686..184719478hg38UCSC Ensembl
Innerchr1:184615382..184683491hg19UCSC Ensembl
Outerchr1:184609820..184688612hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3878793
hg1978793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005221
Samples
Known GenesEDEM3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154439
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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