A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740758



Internal ID164424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74251105..74252342hg38UCSC Ensembl
chrX:73470940..73472177hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419260
Supporting Variants
Samples
Known GenesFTX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740758
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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