A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420641



Internal ID22478511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161564247..161564729hg38UCSC Ensembl
chr5:160991253..160991735hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420641
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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