A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950127



Internal ID22725549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173808694..173808694hg38UCSC Ensembl
chr5:173235697..173235697hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950127
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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