A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932552



Internal ID21352621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165749182..165749182hg38UCSC Ensembl
chr6:166162670..166162670hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202939
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932552
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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