A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720440



Internal ID144106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2695889..2699398hg38UCSC Ensembl
chr19:2695887..2699396hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383510
hg193510
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556347
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720440
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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