A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517427



Internal ID20890788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2691819..2698444hg38UCSC Ensembl
chr19:2691817..2698442hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386626
hg196626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046068
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517427
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