A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414789



Internal ID21072342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10658700..10676004hg38UCSC Ensembl
chr6:10658933..10676237hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3817305
hg1917305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136871
Samples
Known GenesC6orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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