A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713198



Internal ID136864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41689941..41690087hg38UCSC Ensembl
chr17:39846193..39846339hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529654
Supporting Variants
Samples
Known GenesEIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713198
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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