A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616487



Internal ID20989558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161517116..161675769hg38UCSC Ensembl
chr6:161938148..162096801hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38158654
hg19158654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216746
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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