A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415343



Internal ID21072896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34478349..34480093hg38UCSC Ensembl
chr6:34446126..34447870hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141667
Samples
Known GenesPACSIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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