A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367486



Internal ID21025039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29566348..29603400hg38UCSC Ensembl
chr4:29567970..29605022hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3837053
hg1937053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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