A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112507



Internal ID22021740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152810767..152936044hg38UCSC Ensembl
chrX:151979299..152104588hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38125278
hg19125290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642267
Samples
Known GenesCETN2, NSDHL, ZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112507
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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