A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414639



Internal ID21072192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91628091..91628584hg38UCSC Ensembl
chr6:92337809..92338302hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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