A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279070



Internal ID20488288
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 StatusS
Merged Variantsnsv4764193
Supporting Variants
Samples
Known GenesMAOB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279070
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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