A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357092



Internal ID21014645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6661087..6667114hg38UCSC Ensembl
chr4:6662814..6668841hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386028
hg196028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357092
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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