A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403475



Internal ID21061028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10267771..10270730hg38UCSC Ensembl
chr6:10268004..10270963hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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