A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399900



Internal ID179286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9284563..9284614hg38UCSC Ensembl
chr10:9326526..9326577hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032396
Samples
Known GenesLINC00709
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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