A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321917



Internal ID20855026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222077579..222081389hg38UCSC Ensembl
chr1:222250921..222254731hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383811
hg193811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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