A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444766



Internal ID21102319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29207734..29239852hg38UCSC Ensembl
chr11:29229281..29261399hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3832119
hg1932119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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