A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875723



Internal ID22650681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24284726..24286052hg38UCSC Ensembl
chrX:24302843..24304169hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2272n209
Supporting Variantsnssv17455235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875723
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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