A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495467



Internal ID21153020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79541001..79542100hg38UCSC Ensembl
chr13:80115136..80116235hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013480
Samples
Known GenesNDFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495467
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