A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614741



Internal ID20987812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98605667..98605910hg38UCSC Ensembl
chr6:99053543..99053786hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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