A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645027



Internal ID21837074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040676..45040729hg38UCSC Ensembl
chrX:44899921..44899974hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110792
Supporting Variants
Samples
Known GenesKDM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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