A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740095



Internal ID163761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37495204..37508812hg38UCSC Ensembl
chrX:37354457..37368065hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3813609
hg1913609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740095
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0104102


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