A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345824



Internal ID21003377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149038401..149039800hg38UCSC Ensembl
chr2:149894915..149896314hg19UCSC Ensembl
Cytoband2q23.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205511
Samples
Known GenesLYPD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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