A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239014



Internal ID21686523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21659167..21659167hg38UCSC Ensembl
chr10:21948096..21948096hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714532
Supporting Variants
Samples
Known GenesMLLT10
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)nssv17239014
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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