A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919698



Internal ID22694920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61735551..61735600hg38UCSC Ensembl
chr8:62648110..62648159hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919698
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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