A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394599



Internal ID21052152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137595032..137628628hg38UCSC Ensembl
chr4:138516186..138549782hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3833597
hg1933597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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