A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350621



Internal ID21008174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65555879..65811282hg38UCSC Ensembl
chr2:65783013..66038416hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38255404
hg19255404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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