A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140679



Internal ID339872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95964897..95964959hg38UCSC Ensembl
chr5:95300601..95300663hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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