A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086444



Internal ID20653484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39527033..39528193hg38UCSC Ensembl
chr2:39754174..39755334hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349845
Supporting Variants
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00362


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