A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493099



Internal ID21150652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90368001..90369500hg38UCSC Ensembl
chr13:91020255..91021754hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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