A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042542



Internal ID21951858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41262209..41262209hg38UCSC Ensembl
chrX:41121462..41121462hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042542
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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