A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319476



Internal ID20852571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119125935..119126467hg38UCSC Ensembl
chr1:119668558..119669090hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200361
Samples
Known GenesWARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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