A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404786



Internal ID21062339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65810257..65811601hg38UCSC Ensembl
chr5:65106084..65107428hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214830
Samples
Known GenesNLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404786
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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