A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333784



Internal ID20866965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28827973..28831713hg38UCSC Ensembl
chr1:29154485..29158225hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383741
hg193741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059985
Samples
Known GenesOPRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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