A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335462



Internal ID20868654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160300627..160304535hg38UCSC Ensembl
chr1:160270417..160274325hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg383909
hg193909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052450
Samples
Known GenesCOPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335462
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