A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643765



Internal ID21835812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133419182..133419235hg38UCSC Ensembl
chrX:132553210..132553263hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643765
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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