A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5396625



Internal ID176040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28716299..28716350hg38UCSC Ensembl
chr10:29005228..29005279hg19UCSC Ensembl
Cytoband10p12.1
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 Variantsnssv17033434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5396625
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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