A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968468



Internal ID22743403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2590120..2601012hg38UCSC Ensembl
chrX:2508161..2519053hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3810893
hg1910893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968468
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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