A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393820



Internal ID21051373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44786861..44787430hg38UCSC Ensembl
chr4:44788878..44789447hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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