A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440120



Internal ID21097673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5561496..5613774hg38UCSC Ensembl
chr10:5603459..5655737hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3852279
hg1952279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440120
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