A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973383



Internal ID22748319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51282480..51302501hg38UCSC Ensembl
chrX:51025337..51045353hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3820022
hg1920017
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973383
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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