A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951633



Internal ID21371495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24921587..24921587hg38UCSC Ensembl
chr8:24779100..24779100hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204649
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951633
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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