A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397456



Internal ID21055009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5130201..5433200hg38UCSC Ensembl
chr6:5130435..5433433hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38303000
hg19302999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6048n223
Supporting Variantsnssv18145039
Samples
Known GenesFARS2, LYRM4, MIR3691
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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