A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319811



Internal ID20852908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225950718..225952793hg38UCSC Ensembl
chr1:226138418..226140493hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg382076
hg192076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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