A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446051



Internal ID21103604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6428577..6437175hg38UCSC Ensembl
chr11:6449807..6458405hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388599
hg198599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993842
Samples
Known GenesHPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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