A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264572



Internal ID20473790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3090752..3091657hg38UCSC Ensembl
chr6:3090986..3091891hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738903
Supporting Variants
Samples
Known GenesRIPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264572
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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