A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714338



Internal ID138004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70577327..70579699hg38UCSC Ensembl
chr17:68573468..68575840hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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