A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412522



Internal ID21070075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41788364..41788711hg38UCSC Ensembl
chr6:41756102..41756449hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143339
Samples
Known GenesTOMM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412522
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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