A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370582



Internal ID21028135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18429627..18430093hg38UCSC Ensembl
chr4:18431250..18431716hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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