A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328771



Internal ID20861921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13837001..13841800hg38UCSC Ensembl
chr1:14163496..14168295hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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