A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722666



Internal ID146332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29715712..29715712hg38UCSC Ensembl
chr19:30206619..30206619hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560198
Supporting Variants
Samples
Known GenesC19orf12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722666
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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