A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385007



Internal ID21042560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54453578..54462540hg38UCSC Ensembl
chr4:55319745..55328707hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg388963
hg198963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer