A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980276



Internal ID22755211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88296044..88345280hg38UCSC Ensembl
chrX:87551045..87600281hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3849237
hg1949237
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980276
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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