A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056171



Internal ID20623212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19782244..19783567hg38UCSC Ensembl
chr1:20108737..20110060hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334616
Supporting Variants
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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