A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138523



Internal ID337707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154555606..154689606hg38UCSC Ensembl
chrX:153783821..153917881hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38134001
hg19134061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738133
Samples
Known GenesCTAG1A, CTAG1B, CTAG2, FAM223A, FAM223B, GAB3, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138523
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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