A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974109



Internal ID22749044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93053251..93068970hg38UCSC Ensembl
chrX:92308250..92323969hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3815720
hg1915720
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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