A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830729



Internal ID22605664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6556597..6575504hg38UCSC Ensembl
chr1:6616657..6635564hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3818908
hg1918908
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481140
Samples
Known GenesTAS1R1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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