A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764193



Internal ID20540053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43857135..43857201hg38UCSC Ensembl
chrX:43716381..43716447hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279070
Samples
Known GenesMAOB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764193
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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