A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17233445



Internal ID21680954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8663975..8663975hg38UCSC Ensembl
chr12:8816571..8816571hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728878
Supporting Variants
Samples
Known Genes
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)nssv17233445
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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