A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648722



Internal ID21840769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040143..45040453hg38UCSC Ensembl
chrX:44899388..44899698hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108245
Supporting Variants
Samples
Known GenesKDM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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