A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736161



Internal ID159827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4597488..4946000hg38UCSC Ensembl
chrX:4515529..4864041hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38348513
hg19348513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736161
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627221


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