A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606121



Internal ID21554426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4117454..4117454hg38UCSC Ensembl
chrX:4035495..4035495hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167772
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606121
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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