A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739214



Internal ID162880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10032830..10032979hg38UCSC Ensembl
chrX:10000870..10001019hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414679
Supporting Variants
Samples
Known GenesWWC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.204759


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