A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737759



Internal ID161425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145993252..145994657hg38UCSC Ensembl
chrX:145074770..145076175hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420852
Supporting Variants
Samples
Known GenesMIR890
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003435


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