A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740736



Internal ID164402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73786749..74066861hg38UCSC Ensembl
chrX:73006584..73286696hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38280113
hg19280113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427810
Supporting Variants
Samples
Known GenesFTX, JPX, TSIX, XIST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000832466


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