A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462836



Internal ID22520721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2776581..2890877hg38UCSC Ensembl
chrX:2694622..2808918hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38114297
hg19114297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875720
Supporting Variants
Samples
Known GenesGYG2, XG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462836
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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