A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349391



Internal ID21006944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:140329046..140331844hg38UCSC Ensembl
chr2:141086615..141089413hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg382799
hg192799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206629
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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