A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742708



Internal ID166374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140930528..140936388hg38UCSC Ensembl
chrX:140012693..140018553hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg385861
hg195861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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