A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398019



Internal ID21055572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95239501..95240500hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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