A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928632



Internal ID21348701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683759..24683759hg38UCSC Ensembl
chr6:24683987..24683987hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202356
SamplesHG002
Known GenesACOT13
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928632
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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