A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327263



Internal ID20860400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87215150..87215866hg38UCSC Ensembl
chr1:87680833..87681549hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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