A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339075



Internal ID20996628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190621601..190667200hg38UCSC Ensembl
chr2:191486327..191531926hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3845600
hg1945600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205427
Samples
Known GenesNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339075
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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