A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138942



Internal ID338126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102188542..102234700hg38UCSC Ensembl
chrX:101443515..101489694hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3846159
hg1946180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741754
Samples
Known GenesTCP11X2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138942
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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