A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493899



Internal ID21151452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41368654..41424202hg38UCSC Ensembl
chr13:41942790..41998338hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3855549
hg1955549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008948
Samples
Known GenesNAA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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