A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477698



Internal ID255269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8086669..8087853hg38UCSC Ensembl
chr10:8128632..8129816hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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