A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968426



Internal ID22743361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20465149..20478144hg38UCSC Ensembl
chrX:20483267..20496262hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3812996
hg1912996
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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