A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910034



Internal ID22685244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76920571..76923701hg38UCSC Ensembl
chr8:77832807..77835937hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383131
hg193131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910034
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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