A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415792



Internal ID195040
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 StatusM
Merged Variants
Supporting Variantsnssv17737300
Samples
Known GenesLONRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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