A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530997



Internal ID306962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57507631..57512164hg38UCSC Ensembl
chr17:55584992..55589525hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724862
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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