A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475961



Internal ID21133514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65315201..65325200hg38UCSC Ensembl
chr14:65781919..65791918hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475961
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