A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412663



Internal ID21070216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149447802..149470841hg38UCSC Ensembl
chr5:148827365..148850404hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3823040
hg1923040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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