A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971335



Internal ID48235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90479596..90917865hg38UCSC Ensembl
chr5:89775413..90213682hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38438270
hg19438270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463778
Supporting Variants
Samples
Known GenesGPR98, LYSMD3, POLR3G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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