A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351322



Internal ID21008875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46589601..46590500hg38UCSC Ensembl
chr2:46816740..46817639hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089952
Samples
Known GenesPIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351322
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