A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967828



Internal ID22742763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1433585..1446976hg38UCSC Ensembl
chrX:1552478..1565869hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3813392
hg1913392
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515578
Samples
Known GenesASMTL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967828
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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