A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920959



Internal ID22696182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127646070..127652477hg38UCSC Ensembl
chr8:128658315..128664722hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386408
hg196408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920959
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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