A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352676



Internal ID21010229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231404207..231437823hg38UCSC Ensembl
chr2:232268918..232302534hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3833617
hg1933617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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