A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357186



Internal ID21014739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35024801..35056000hg38UCSC Ensembl
chr4:35026423..35057622hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3831200
hg1931200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5228n223
Supporting Variantsnssv18213520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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