A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978643



Internal ID53134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173031324..173038000hg38UCSC Ensembl
chr5:172458327..172465003hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386677
hg196677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454395
Supporting Variants
Samples
Known GenesATP6V0E1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978643
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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