A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740689



Internal ID164355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72264263..72266795hg38UCSC Ensembl
chrX:71484113..71486645hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg382533
hg192533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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