A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393523



Internal ID21051076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42239845..42240545hg38UCSC Ensembl
chr5:42239947..42240647hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393523
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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