A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342297



Internal ID20999850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219561347..219571478hg38UCSC Ensembl
chr2:220426069..220436200hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3810132
hg1910132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205642
Samples
Known GenesOBSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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