A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436568



Internal ID21094121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28704455..28767952hg38UCSC Ensembl
chr11:28726002..28789499hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3863498
hg1963498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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