A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741542



Internal ID165208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94762571..94762571hg38UCSC Ensembl
chrX:94017570..94017570hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741542
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00100125


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