A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318561



Internal ID20851653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20596289..20618782hg38UCSC Ensembl
chr1:20922782..20945275hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3822494
hg1922494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199872
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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