A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959057



Internal ID22734102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61794266..61794266hg38UCSC Ensembl
chr8:62706825..62706825hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959057
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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