A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521989



Internal ID20895350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50960960..50961329hg38UCSC Ensembl
chr19:51464216..51464585hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048698
Samples
Known GenesKLK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521989
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