A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929172



Internal ID21349241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52064234..52064234hg38UCSC Ensembl
chr8:52976794..52976794hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204075
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929172
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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