A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17251700



Internal ID21699209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17670793..17670793hg38UCSC Ensembl
chr10:17712792..17712792hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722818
Supporting Variants
Samples
Known GenesSTAM
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)nssv17251700
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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