A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405939



Internal ID21063492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47656803..47658262hg38UCSC Ensembl
chr6:47624539..47625998hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144922
Samples
Known GenesGPR111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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