A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051229



Internal ID21960462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49945742..49945742hg38UCSC Ensembl
chrX:49710352..49710352hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642199
Samples
Known GenesCLCN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051229
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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