A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711869



Internal ID135535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17687954..17688353hg38UCSC Ensembl
chr17:17591268..17591667hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145507
Supporting Variants
Samples
Known GenesRAI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711869
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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