A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358103



Internal ID21015656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31667087..31735475hg38UCSC Ensembl
chr4:31668709..31737097hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3868389
hg1968389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5218n223
Supporting Variantsnssv18214672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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