A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424051



Internal ID22481921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165070659..165077229hg38UCSC Ensembl
chr5:164497665..164504235hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386571
hg196571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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