A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369302



Internal ID21026855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36620163..36620972hg38UCSC Ensembl
chr3:36661655..36662464hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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