A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740069



Internal ID163735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36578745..36841831hg38UCSC Ensembl
chrX:36596819..36859904hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38263087
hg19263086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740069
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062435


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