A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978131



Internal ID22753066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80950863..80978239hg38UCSC Ensembl
chrX:80206362..80233738hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3827377
hg1927377
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978131
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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