A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968744



Internal ID22743679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142765925..142772367hg38UCSC Ensembl
chrX:141853711..141860153hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg386443
hg196443
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968744
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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