A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971523



Internal ID22746458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:754084..764079hg38UCSC Ensembl
chrX:714819..724814hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389996
hg199996
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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