A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405777



Internal ID21063330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149302970..149309698hg38UCSC Ensembl
chr5:148682533..148689261hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386729
hg196729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213274
Samples
Known GenesAFAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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