A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487881



Internal ID21145434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109704782..109734274hg38UCSC Ensembl
chr13:110357129..110386621hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3829493
hg1929493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007975
Samples
Known GenesLINC00676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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