A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411357



Internal ID21068910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66179328..66255938hg38UCSC Ensembl
chr5:65475156..65551766hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3876611
hg1976611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214842
Samples
Known GenesSREK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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