A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519626



Internal ID20892987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44272509..44276104hg38UCSC Ensembl
chr19:44776662..44780257hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383596
hg193596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048151
Samples
Known GenesZNF233
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519626
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