A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080700



Internal ID20647740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186764501..186765400hg38UCSC Ensembl
chr2:187629228..187630127hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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