A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494300



Internal ID21151853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88734001..88734900hg38UCSC Ensembl
chr13:89386255..89387154hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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