A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978183



Internal ID22753118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119370533..119391755hg38UCSC Ensembl
chrX:118504496..118525718hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3821223
hg1921223
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515253, nssv17515254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978183
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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