A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954379



Internal ID21374449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73205683..73205683hg38UCSC Ensembl
chr6:73915406..73915406hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202830
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954379
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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