A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138505



Internal ID337689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:34147329..34147405hg38UCSC Ensembl
chrX:34165446..34165522hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138505
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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