A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288783



Internal ID20498001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113172987..113173065hg38UCSC Ensembl
chrX:112416214..112416292hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288783
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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