A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086447



Internal ID20653487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39580022..39604014hg38UCSC Ensembl
chr2:39807162..39831154hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3823993
hg1923993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347862
Supporting Variants
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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