A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952522



Internal ID22727835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38203171..38203171hg38UCSC Ensembl
chr5:38203273..38203273hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952522
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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