A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477714



Internal ID255285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48365048..48366910hg38UCSC Ensembl
chr8:49277608..49279470hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381863
hg191863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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