A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345550



Internal ID21003103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1971305..1979204hg38UCSC Ensembl
chr2:1975077..1982976hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208248
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345550
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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