A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288744



Internal ID20497962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65369796..65373269hg38UCSC Ensembl
chrX:64589676..64593149hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg383474
hg193474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288744
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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