A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879379



Internal ID22654348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52374715..52375088hg38UCSC Ensembl
chrX:52117858..52118231hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454739
Samples
Known GenesXAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879379
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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