A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411842



Internal ID21069395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61405701..61410700hg38UCSC Ensembl
chr5:60701528..60706527hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216258
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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