A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333956



Internal ID20867137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198778601..198816376hg38UCSC Ensembl
chr1:198747730..198785505hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3837776
hg1937776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056822
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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