A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924107



Internal ID22699334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62154037..62177442hg38UCSC Ensembl
chr8:63066596..63090001hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3823406
hg1923406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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