A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561998



Internal ID21886353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3105303..3105303hg38UCSC Ensembl
chr6:3105537..3105537hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381967
hg191967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067609
Supporting Variants
Samples
Known GenesRIPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561998
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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