A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574163



Internal ID21766206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3093958..3093958hg38UCSC Ensembl
chr6:3094192..3094192hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073311
Supporting Variants
Samples
Known GenesRIPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574163
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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