A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085907



Internal ID20652947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21848724..21849020hg38UCSC Ensembl
chr2:22071596..22071892hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00186


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