A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739473



Internal ID163139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17537919..17538058hg38UCSC Ensembl
chrX:17556041..17556180hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425703
Supporting Variants
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739473
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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