A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373669



Internal ID21031222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65467735..67235725hg38UCSC Ensembl
chr3:65453410..67286149hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381767991
hg191832740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212972
Samples
Known GenesKBTBD8, LRIG1, MAGI1, MAGI1-AS1, MIR4272, SLC25A26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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