A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383645



Internal ID21041198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35894718..35896394hg38UCSC Ensembl
chr5:35894820..35896496hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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