A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885654



Internal ID22660639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100998704..101006536hg38UCSC Ensembl
chrX:100253693..100261525hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg387833
hg197833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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