A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736755



Internal ID160421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46495973..46497337hg38UCSC Ensembl
chrX:46355408..46356772hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736755
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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