A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357389



Internal ID21014942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71899005..71899546hg38UCSC Ensembl
chr3:71948156..71948697hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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