A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888048



Internal ID22663048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98467705..98469681hg38UCSC Ensembl
chr5:97803409..97805385hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381977
hg191977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888048
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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