A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523522



Internal ID299751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28329981..28330097hg38UCSC Ensembl
chr17:26657007..26657123hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712349
Samples
Known GenesIFT20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523522
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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