A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640692



Internal ID21832739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55749160..55749211hg38UCSC Ensembl
chrX:55775593..55775644hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109966
Supporting Variants
Samples
Known GenesRRAGB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640692
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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