A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336941



Internal ID20994494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226341957..226365671hg38UCSC Ensembl
chr2:227206673..227230387hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3823715
hg1923715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336941
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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