A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714575



Internal ID138241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74757874..74757954hg38UCSC Ensembl
chr17:72754013..72754093hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518134
Supporting Variants
Samples
Known GenesSLC9A3R1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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