A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372039



Internal ID21029592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132269201..132276400hg38UCSC Ensembl
chr3:131988045..131995244hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5021n223
Supporting Variantsnssv18094161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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