A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354559



Internal ID21012112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65075658..65084886hg38UCSC Ensembl
chr2:65302792..65312020hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389229
hg199229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206951
Samples
Known GenesCEP68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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