A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334495



Internal ID20867681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11924701..11926500hg38UCSC Ensembl
chr1:11984758..11986557hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200362
Samples
Known GenesKIAA2013
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334495
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