A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411490



Internal ID21069043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95926270..95927811hg38UCSC Ensembl
chr6:96374146..96375687hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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