A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736577



Internal ID160243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41501015..41507920hg38UCSC Ensembl
chrX:41360268..41367173hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg386906
hg196906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736577
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0119048


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