A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941255



Internal ID21361324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71316324..71316324hg38UCSC Ensembl
chr6:72026027..72026027hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202818
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941255
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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