A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413142



Internal ID21070695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86469979..86640609hg38UCSC Ensembl
chr6:87179697..87350327hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38170631
hg19170631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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