A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416886



Internal ID22474756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157242425..157243006hg38UCSC Ensembl
chr5:156669435..156670016hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901926
Supporting Variants
Samples
Known GenesITK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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