A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319026



Internal ID20852118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157942043..157942567hg38UCSC Ensembl
chr1:157911833..157912357hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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