A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415556



Internal ID21073109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65729626..65730804hg38UCSC Ensembl
chr5:65025453..65026631hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214829
Samples
Known GenesNLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415556
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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