A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952766



Internal ID21372835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124455067..124455067hg38UCSC Ensembl
chr8:125467308..125467308hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204988
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952766
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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