A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574547



Internal ID21766590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160748350..160748350hg38UCSC Ensembl
chr6:161169382..161169382hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071362
Supporting Variants
Samples
Known GenesPLG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574547
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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