A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380198



Internal ID21037751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120985648..121315408hg38UCSC Ensembl
chr4:121906803..122236563hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38329761
hg19329761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210214
Samples
Known GenesNDNF, TNIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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