A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110060



Internal ID22019293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150690018..150693838hg38UCSC Ensembl
chrX:149858491..149862311hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638395
Samples
Known GenesMTMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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