A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875239



Internal ID22650196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24311767..24311817hg38UCSC Ensembl
chrX:24329884..24329934hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450731
Samples
Known GenesSUPT20HL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875239
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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