A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869623



Internal ID22644559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115688357..115720718hg38UCSC Ensembl
chrX:114922677..114955038hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3832362
hg1932362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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