A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521577



Internal ID20894938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58197586..58201427hg38UCSC Ensembl
chr18:55864818..55868659hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg383842
hg193842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042317
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521577
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