A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089131



Internal ID20656171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38207067..38208608hg38UCSC Ensembl
chr2:38434209..38435750hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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