A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056770



Internal ID21966004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040278..45040278hg38UCSC Ensembl
chrX:44899523..44899523hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638126
Samples
Known GenesKDM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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