A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737300



Internal ID160966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118981604..118981682hg38UCSC Ensembl
chrX:118115567..118115645hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415792
Supporting Variants
Samples
Known GenesLONRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737300
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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