A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975954



Internal ID51367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157548967..157551176hg38UCSC Ensembl
chr5:156975975..156978184hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466261
Supporting Variants
Samples
Known GenesADAM19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975954
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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