A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873332



Internal ID22648278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19134694..19160403hg38UCSC Ensembl
chrX:19152812..19178521hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3825710
hg1925710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873332
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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