A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563638



Internal ID21887993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165618931..165619693hg38UCSC Ensembl
chr6:166032419..166033181hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008751
Supporting Variants
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563638
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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