A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366170



Internal ID21023723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73114594..73179757hg38UCSC Ensembl
chr3:73163745..73228908hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3865164
hg1965164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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