A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321088



Internal ID20854190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26097329..26103753hg38UCSC Ensembl
chr1:26423820..26430244hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386425
hg196425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321088
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