A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239806



Internal ID21687315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25637915..25637915hg38UCSC Ensembl
chr1:25964406..25964406hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5727436
Supporting Variants
Samples
Known GenesMAN1C1
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)nssv17239806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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