A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399875



Internal ID21057428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34179928..34230366hg38UCSC Ensembl
chr6:34147705..34198143hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3850439
hg1950439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399875
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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