A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107470



Internal ID22016703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146809812..146813184hg38UCSC Ensembl
chrX:145891330..145894702hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg383373
hg193373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647528
Samples
Known GenesCXorf51A, CXorf51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107470
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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