A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17238932



Internal ID21686441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35762729..35762729hg38UCSC Ensembl
chr19:36253630..36253630hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723538
Supporting Variants
Samples
Known GenesC19orf55
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)nssv17238932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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