A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325103



Internal ID20858233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69683212..69720736hg38UCSC Ensembl
chr1:70148895..70186419hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3837525
hg1937525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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