A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271708



Internal ID20480926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66757470..66757743hg38UCSC Ensembl
chrX:65977312..65977585hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271708
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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