A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338327



Internal ID20995880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82695794..82743388hg38UCSC Ensembl
chr2:82922918..82970512hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3847595
hg1947595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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