A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465176



Internal ID243045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31729451..31739763hg38UCSC Ensembl
chr5:31729558..31739870hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3810313
hg1910313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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