A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527436



Internal ID303537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55345099..55345218hg38UCSC Ensembl
chr19:55856467..55856586hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725660
Samples
Known GenesSUV420H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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