A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740590



Internal ID164256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70007826..70007904hg38UCSC Ensembl
chrX:69227676..69227754hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421078
Supporting Variants
Samples
Known GenesEDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740590
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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