A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873692



Internal ID22648640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45836197..45836503hg38UCSC Ensembl
chrX:45695624..45695928hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38307
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873692
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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