A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666485



Internal ID21614790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103601765..103603776hg38UCSC Ensembl
chrX:102856693..102858704hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg382012
hg192012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165179
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666485
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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