A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715606



Internal ID139272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81722543..81725804hg38UCSC Ensembl
chr17:79689573..79692834hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383262
hg193262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008284


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