A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740822



Internal ID164488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76110322..76122776hg38UCSC Ensembl
chrX:75330157..75342611hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3812455
hg1912455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740822
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000416233


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