A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040997



Internal ID20608037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3421958..3423406hg38UCSC Ensembl
chr18:3421956..3423404hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527396
Supporting Variants
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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