A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482429



Internal ID21139982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74748236..74756420hg38UCSC Ensembl
chr13:75322373..75330557hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg388185
hg198185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer