A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408718



Internal ID21066271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165635658..165727227hg38UCSC Ensembl
chr5:165062663..165154232hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3891570
hg1991570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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