A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087113



Internal ID20654153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:50346601..50347100hg38UCSC Ensembl
chr2:50573739..50574238hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346556
Supporting Variants
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08334


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