A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142740



Internal ID20709780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40408626..40413359hg38UCSC Ensembl
chr6:40376365..40381098hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407582
Supporting Variants
Samples
Known GenesLRFN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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