A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720792



Internal ID144458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4965547..4965847hg38UCSC Ensembl
chr19:4965558..4965858hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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