A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710886



Internal ID134552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2009106..2010239hg38UCSC Ensembl
chr17:1912400..1913533hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517798
Supporting Variants
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.347175


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