A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063446



Internal ID20630486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69060900..69062338hg38UCSC Ensembl
chr1:69526583..69528021hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg381439
hg191439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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