A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640388



Internal ID21832435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113181466..113181747hg38UCSC Ensembl
chrX:112424693..112424974hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640388
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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