A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346881



Internal ID21004434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73701938..73718398hg38UCSC Ensembl
chr2:73929065..73945525hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg3816461
hg1916461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346881
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