A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980023



Internal ID22754958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73107833..73119482hg38UCSC Ensembl
chrX:72327672..72339321hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3811650
hg1911650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516709, nssv17516710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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