A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530180



Internal ID20903541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12105529..12108976hg38UCSC Ensembl
chr18:12105528..12108975hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3283n223
Supporting Variantsnssv18038762
Samples
Known GenesANKRD62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530180
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