A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741852



Internal ID165518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107089600..107095300hg38UCSC Ensembl
chrX:106332830..106338530hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138124
Supporting Variants
Samples
Known GenesRBM41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00230802


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