A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318959



Internal ID20852051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79191507..79298740hg38UCSC Ensembl
chr1:79657192..79764425hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38107234
hg19107234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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