A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213561



Internal ID20780601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38800701..38839500hg38UCSC Ensembl
chr4:38802322..38841121hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3838800
hg1938800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387241
Supporting Variants
Samples
Known GenesTLR1, TLR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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