A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714581



Internal ID138247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74877359..74881651hg38UCSC Ensembl
chr17:72873488..72877781hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384293
hg194294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518456
Supporting Variants
Samples
Known GenesFADS6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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