A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644927



Internal ID21836974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22550394..22601602hg38UCSC Ensembl
chrX:22568511..22619719hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3851209
hg1951209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108396
Supporting Variants
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644927
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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