A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737312



Internal ID160978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119207466..119209271hg38UCSC Ensembl
chrX:118341429..118343234hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381806
hg191806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737312
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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