A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916900



Internal ID22692119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126572752..126574405hg38UCSC Ensembl
chr8:127584997..127586650hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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