A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138580



Internal ID337764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154557000..154585606hg38UCSC Ensembl
chrX:153785215..153813865hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828607
hg1928651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738134
Samples
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138580
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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