A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415361



Internal ID21072914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51407801..51412800hg38UCSC Ensembl
chr6:51272599..51277598hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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