A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532606



Internal ID20905967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14897526..14911767hg38UCSC Ensembl
chr19:15008338..15022579hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3814242
hg1914242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532606
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