A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317293



Internal ID20850377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36241097..36246691hg38UCSC Ensembl
chr1:36706698..36712292hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385595
hg195595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060731
Samples
Known GenesTHRAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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