A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948259



Internal ID21368328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159898616..159898616hg38UCSC Ensembl
chr6:160319648..160319648hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202128
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948259
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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