A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109959



Internal ID22019192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53578452..53578504hg38UCSC Ensembl
chrX:53605412..53605464hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641843
Samples
Known GenesHUWE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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