A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618866



Internal ID20991937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108133892..108137941hg38UCSC Ensembl
chr6:108455096..108459145hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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