A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444220



Internal ID21101773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11848905..11930549hg38UCSC Ensembl
chr10:11890904..11972548hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3881645
hg1981645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187944
Samples
Known GenesPROSER2, PROSER2-AS1, UPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444220
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