A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493602



Internal ID21151155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88546270..88546724hg38UCSC Ensembl
chr13:89198525..89198979hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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