A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978179



Internal ID22753114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23757988..23771360hg38UCSC Ensembl
chrX:23776105..23789477hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3813373
hg1913373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer