A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604227



Internal ID20977298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154974900..154982514hg38UCSC Ensembl
chr6:155296034..155303648hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg387615
hg197615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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