A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609850



Internal ID20982921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98044354..98044889hg38UCSC Ensembl
chr6:98492230..98492765hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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