A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014637



Internal ID20581677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91088308..91094469hg38UCSC Ensembl
chr13:91740562..91746723hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg386162
hg196162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495432
Supporting Variants
Samples
Known GenesLINC00380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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