A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736928



Internal ID160594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50720141..50720599hg38UCSC Ensembl
chrX:50463141..50463599hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426925
Supporting Variants
Samples
Known GenesSHROOM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736928
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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