A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524944



Internal ID20898305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70002301..70039700hg38UCSC Ensembl
chr18:67669537..67706936hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3837400
hg1937400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043669
Samples
Known GenesRTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524944
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