A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350440



Internal ID21007993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5532217..5541294hg38UCSC Ensembl
chr2:5672349..5681426hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg389078
hg199078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer