A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953648



Internal ID22728926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105908503..105908503hg38UCSC Ensembl
chr8:106920731..106920731hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953648
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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