A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316096



Internal ID20849173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171285638..171288806hg38UCSC Ensembl
chr1:171254777..171257945hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053814
Samples
Known GenesFMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316096
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