A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710872



Internal ID134538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1919636..1919690hg38UCSC Ensembl
chr17:1822930..1822984hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710872
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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