A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010019



Internal ID21919362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59390450..59520177hg38UCSC Ensembl
chr8:60303009..60432736hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38129728
hg19129728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010019
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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