A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978038



Internal ID22752973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66931426..66938085hg38UCSC Ensembl
chrX:66151268..66157927hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg386660
hg196660
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978038
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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