A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347891



Internal ID21005444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68159746..68165672hg38UCSC Ensembl
chr2:68386878..68392804hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg385927
hg195927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088823
Samples
Known GenesPNO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347891
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