A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322666



Internal ID20855779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105423301..105429300hg38UCSC Ensembl
chr1:105965923..105971922hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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