A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566476



Internal ID21758519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42936136..42936136hg38UCSC Ensembl
chr6:42903874..42903874hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073657
Supporting Variants
Samples
Known GenesCNPY3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566476
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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