A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927022



Internal ID21347093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169242634..169242634hg38UCSC Ensembl
chr6:169642729..169642729hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202664
SamplesHG002
Known GenesTHBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927022
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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