A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486992



Internal ID21144545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89337154..89616359hg38UCSC Ensembl
chr13:89989408..90268613hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38279206
hg19279206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015139
Samples
Known GenesLINC00353
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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