A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737368



Internal ID161034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120143917..120143917hg38UCSC Ensembl
chrX:119277823..119277823hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0473552


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