A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345283



Internal ID21002836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90304001..90368200hg38UCSC Ensembl
chr2:90405837..90470036hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3864200
hg1964200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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