A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647379



Internal ID21839426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112972245..112972327hg38UCSC Ensembl
chrX:112215473..112215555hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647379
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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