A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665329



Internal ID21613634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24274583..24274914hg38UCSC Ensembl
chrX:24292700..24293031hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166912
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665329
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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