A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320871



Internal ID20853972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200876907..200884225hg38UCSC Ensembl
chr1:200846035..200853353hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387319
hg197319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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