A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373358



Internal ID21030911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36670234..36677917hg38UCSC Ensembl
chr3:36711725..36719408hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387684
hg197684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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