A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516427



Internal ID292887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35149078..35149215hg38UCSC Ensembl
chr19:35639981..35640118hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722994
Samples
Known GenesFXYD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516427
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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