A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380511



Internal ID21038064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143428959..143495934hg38UCSC Ensembl
chr4:144350112..144417087hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3866976
hg1966976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213081
Samples
Known GenesGAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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