A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477069



Internal ID21134622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44681889..44683625hg38UCSC Ensembl
chr13:45256025..45257761hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477069
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