A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879993



Internal ID22654963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152369371..152369430hg38UCSC Ensembl
chrX:151537843..151537902hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429955
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879993
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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