A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549987



Internal ID323590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30556875..30556875hg38UCSC Ensembl
chr19:31047782..31047782hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722723
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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