A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236055



Internal ID20803095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25328551..25358616hg38UCSC Ensembl
chr6:25328779..25358844hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3830066
hg1930066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410442
Supporting Variants
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236055
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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