A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741754



Internal ID165420
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 StatusS
Merged Variantsnsv6138942
Supporting Variants
Samples
Known GenesTCP11X2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741754
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000209556


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