A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112159



Internal ID22021393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77834168..77834234hg38UCSC Ensembl
chrX:77089665..77089731hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648787
Samples
Known GenesMAGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112159
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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