A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340640



Internal ID20998193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36562701..36565900hg38UCSC Ensembl
chr2:36789844..36793043hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089048
Samples
Known GenesFEZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340640
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