A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532729



Internal ID20906090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73599634..73600389hg38UCSC Ensembl
chr18:71266869..71267624hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532729
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