A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138061



Internal ID337243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6417488..6533800hg38UCSC Ensembl
chrX:6335529..6451841hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38116313
hg19116313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739063
Samples
Known GenesVCX3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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