A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482983



Internal ID21140536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35574143..35578835hg38UCSC Ensembl
chr13:36148280..36152972hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384693
hg194693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008349
Samples
Known GenesMIR548F5, NBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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