A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316943



Internal ID20850025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:242780199..242788560hg38UCSC Ensembl
chr1:242943501..242951862hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg388362
hg198362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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