A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882622



Internal ID22657599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43161056..43163123hg38UCSC Ensembl
chr17:41313073..41315140hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382068
hg192068
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882622
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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