A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712585



Internal ID136251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31595164..31595385hg38UCSC Ensembl
chr17:29922183..29922404hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712585
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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