A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328686



Internal ID20861835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43718924..43721471hg38UCSC Ensembl
chr1:44184595..44187142hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061361
Samples
Known GenesST3GAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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