A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336455



Internal ID20994008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216218605..216219170hg38UCSC Ensembl
chr2:217083328..217083893hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085760
Samples
Known GenesPKI55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336455
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