A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440928



Internal ID21098481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19434601..19437600hg38UCSC Ensembl
chr11:19456148..19459147hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988713
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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