A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138678



Internal ID337862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56034000..56176964hg38UCSC Ensembl
chrX:56060433..56203397hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38142965
hg19142965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138678
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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