A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519251



Internal ID295604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2849067..2849458hg38UCSC Ensembl
chr19:2849065..2849456hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720472
Samples
Known GenesZNF555
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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