A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517889



Internal ID20891250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12749301..12752400hg38UCSC Ensembl
chr18:12749300..12752399hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517889
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