A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637953



Internal ID21830000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100972471..100972471hg38UCSC Ensembl
chrX:100227460..100227460hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043532
Supporting Variants
Samples
Known GenesARL13A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637953
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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