A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329516



Internal ID20862668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190908354..191047451hg38UCSC Ensembl
chr1:190877484..191016581hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38139098
hg19139098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv479n223
Supporting Variantsnssv18055729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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