A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542726



Internal ID20915984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14256979..14327818hg38UCSC Ensembl
chr21:15629300..15700139hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3870840
hg1970840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203759
Samples
Known GenesABCC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542726
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