A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440108



Internal ID21097661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19658332..19661758hg38UCSC Ensembl
chr11:19679878..19683304hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383427
hg193427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988723
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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