A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352625



Internal ID21010178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202341851..202358992hg38UCSC Ensembl
chr2:203206574..203223715hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3817142
hg1917142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352625
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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