A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392352



Internal ID21049905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47408968..47420882hg38UCSC Ensembl
chr4:47410985..47422899hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3811915
hg1911915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214311
Samples
Known GenesGABRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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