A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870025



Internal ID22644960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24932007..24932141hg38UCSC Ensembl
chrX:24950124..24950258hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469530
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870025
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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