A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137926



Internal ID337107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116945566..116970000hg38UCSC Ensembl
chrX:116079534..116103968hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3824435
hg1924435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137926
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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