A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410524



Internal ID21068077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46474282..46474787hg38UCSC Ensembl
chr6:46442019..46442524hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144228
Samples
Known GenesRCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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