A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138417



Internal ID337601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64498542..64516885hg38UCSC Ensembl
chrX:63718422..63736765hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3818344
hg1918344
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138417
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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