A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555004



Internal ID328172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30554030..30554030hg38UCSC Ensembl
chr19:31044937..31044937hg19UCSC 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 Variantsnssv17722721
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555004
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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