A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564899



Internal ID21889254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150414531..150414531hg38UCSC Ensembl
chr6:150735667..150735667hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564899
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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