A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426226



Internal ID21083779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155630184..155762735hg38UCSC Ensembl
chr7:155422878..155555429hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38132552
hg19132552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218393
Samples
Known GenesRBM33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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