A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937564



Internal ID21357634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161646345..161646345hg38UCSC Ensembl
chr6:162067377..162067377hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202907
SamplesHG002
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937564
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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