A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745906



Internal ID20521917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53503129..53503129hg38UCSC Ensembl
chrX:53530112..53530112hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745906
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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