A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366784



Internal ID21024337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66994301..68395700hg38UCSC Ensembl
chr3:67044725..68444850hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381401400
hg191400126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103601
Samples
Known GenesFAM19A1, KBTBD8, MIR4272, SUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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