A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638975



Internal ID21831022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121199132..121199189hg38UCSC Ensembl
chrX:120332986..120333043hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638975
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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