A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17237226



Internal ID21684735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43050522..43050522hg38UCSC Ensembl
chr6:43018260..43018260hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5726005
Supporting Variants
Samples
Known GenesCUL7
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17237226
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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