A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667241



Internal ID21615548
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 Variantsnssv17166914
SamplesHG00171
Known GenesSUPT20HL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667241
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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