A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361913



Internal ID21019466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28897922..28914062hg38UCSC Ensembl
chr4:28899544..28915684hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3816141
hg1916141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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