A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638336



Internal ID21830383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132610869..132611295hg38UCSC Ensembl
chrX:131744897..131745323hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638336
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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