A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349702



Internal ID21007255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228585001..228589300hg38UCSC Ensembl
chr2:229449717..229454016hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4302n223
Supporting Variantsnssv18206160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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