A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560198



Internal ID333211
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 StatusM
Merged Variants
Supporting Variantsnssv17722666
Samples
Known GenesC19orf12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560198
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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