A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968614



Internal ID46395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82459807..82466000hg38UCSC Ensembl
chr5:81755626..81761819hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg386194
hg196194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968614
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001718


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