A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519559



Internal ID20892920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37008301..37080201hg38UCSC Ensembl
chr18:34588264..34660164hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3871901
hg1971901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040425
Samples
Known GenesKIAA1328
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519559
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