A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718179



Internal ID21744500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72931589..72931589hg38UCSC Ensembl
chr7:72402127..72402127hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17251952
Samples
Known GenesPOM121
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)nsv5718179
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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