A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926144



Internal ID22701371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133757569..133757645hg38UCSC Ensembl
chr8:134769812..134769888hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926144
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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