A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927488



Internal ID21347557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112573215..112573215hg38UCSC Ensembl
chr6:112894417..112894417hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202578
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927488
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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