A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334861



Internal ID20868050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47158345..47170145hg38UCSC Ensembl
chr1:47624017..47635817hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3811801
hg1911801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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