A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962622



Internal ID22737557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120923880..120923880hg38UCSC Ensembl
chr4:121845035..121845035hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962622
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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