A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087004



Internal ID20654044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226502401..226694400hg38UCSC Ensembl
chr2:227367117..227559116hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38192000
hg19192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340595
Supporting Variants
Samples
Known GenesMIR5702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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