A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375066



Internal ID21032619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32238504..32310373hg38UCSC Ensembl
chr4:32240126..32311995hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3871870
hg1971870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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