A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040613



Internal ID21949956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2228231..2228231hg38UCSC Ensembl
chrX:2146272..2146272hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638850
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040613
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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