A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376433



Internal ID21033986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52302301..52304200hg38UCSC Ensembl
chr4:53168467..53170366hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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