A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712349



Internal ID136015
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 StatusS
Merged Variantsnsv5523522
Supporting Variants
Samples
Known GenesIFT20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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