A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342381



Internal ID20999934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241888701..242102800hg38UCSC Ensembl
chr2:242830852..243044951hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38214100
hg19214100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209035
Samples
Known GenesLOC728323
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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