A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979025



Internal ID22753960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119358905..119367332hg38UCSC Ensembl
chrX:118492868..118501295hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg388428
hg198428
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515250, nssv17515249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979025
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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