A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086390



Internal ID20653430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38779911..38788389hg38UCSC Ensembl
chr2:39007053..39015531hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg388479
hg198479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344523
Supporting Variants
Samples
Known GenesGEMIN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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