A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927277



Internal ID22702505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92867693..92867761hg38UCSC Ensembl
chr8:93879921..93879989hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927277
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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