A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330278



Internal ID20863434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197534101..197571900hg38UCSC Ensembl
chr1:197503231..197541030hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3837800
hg1937800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202316
Samples
Known GenesDENND1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330278
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer