A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439059



Internal ID21096612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10045195..10051114hg38UCSC Ensembl
chr11:10066742..10072661hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385920
hg195920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985078
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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