A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322014



Internal ID20855123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28216153..28218710hg38UCSC Ensembl
chr1:28542664..28545221hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382558
hg192558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203521
Samples
Known GenesDNAJC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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