A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322794



Internal ID20855909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4632540..4633355hg38UCSC Ensembl
chr1:4692600..4693415hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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