A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568124



Internal ID21760167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161646178..161646580hg38UCSC Ensembl
chr6:162067210..162067612hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016663
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568124
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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