A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739047



Internal ID162713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2777488..2891488hg38UCSC Ensembl
chrX:2695529..2809529hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38114001
hg19114001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431134
Supporting Variants
Samples
Known GenesGYG2, XG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739047
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00167259


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