A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875720



Internal ID22650678
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 StatusM
Merged Variants
Supporting Variantsnssv17462836
Samples
Known GenesGYG2, XG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875720
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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