A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409014



Internal ID21066567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41147971..41155533hg38UCSC Ensembl
chr6:41115709..41123271hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387563
hg197563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143317
Samples
Known GenesTREML1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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