A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576997



Internal ID21769040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29460800..29460800hg38UCSC Ensembl
chr6:29428577..29428577hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080386
Supporting Variants
Samples
Known GenesOR2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576997
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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