A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378409



Internal ID21035962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155299271..155302405hg38UCSC Ensembl
chr4:156220423..156223557hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383135
hg193135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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