A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353663



Internal ID21011216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51798662..51872344hg38UCSC Ensembl
chr2:52025800..52099482hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3873683
hg1973683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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