A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876672



Internal ID22651633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119470140..119470364hg38UCSC Ensembl
chrX:118604103..118604327hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444019
Samples
Known GenesSLC25A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876672
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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