A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722968



Internal ID146634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34824920..34863590hg38UCSC Ensembl
chr19:35315824..35354494hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3838671
hg1938671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533770
Supporting Variants
Samples
Known GenesLOC400685
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722968
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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