A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972493



Internal ID22747428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88524762..88539361hg38UCSC Ensembl
chrX:87779763..87794362hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972493
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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