A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138086



Internal ID337268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69788542..69828542hg38UCSC Ensembl
chrX:69008386..69048386hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3840001
hg1940001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740579
Samples
Known GenesEDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138086
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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