A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335046



Internal ID20868237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206052901..206060300hg38UCSC Ensembl
chr1:206281071..206288469hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387400
hg197399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv514n223
Supporting Variantsnssv18199879
Samples
Known GenesC1orf186
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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