A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343132



Internal ID21000685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154850079..154994545hg38UCSC Ensembl
chr2:155706591..155851057hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38144467
hg19144467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205559
Samples
Known GenesKCNJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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