A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531754



Internal ID307701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63821424..63821502hg38UCSC Ensembl
chr17:61898784..61898862hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714028
Samples
Known GenesFTSJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531754
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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