A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737978



Internal ID161644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151311606..151332500hg38UCSC Ensembl
chrX:150480078..150500972hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3820895
hg1920895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00396743


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