A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264556



Internal ID20473774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12744294..12744382hg38UCSC Ensembl
chrX:12762413..12762501hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264556
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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