A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050168



Internal ID21959402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56058262..56058262hg38UCSC Ensembl
chrX:56084695..56084695hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg381967
hg191967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050168
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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