A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925497



Internal ID21345568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166021039..166021039hg38UCSC Ensembl
chr6:166434527..166434527hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202945
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925497
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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