A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381741



Internal ID21039294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107533001..107534800hg38UCSC Ensembl
chr4:108454158..108455957hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5403n223
Supporting Variantsnssv18105795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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