A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051062



Internal ID21960296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040207..45040207hg38UCSC Ensembl
chrX:44899452..44899452hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638667
Samples
Known GenesKDM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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