A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334197



Internal ID20867380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211470479..211478331hg38UCSC Ensembl
chr1:211643821..211651673hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg387853
hg197853
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199929
Samples
Known GenesRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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