A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606180



Internal ID20979251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106084501..106089300hg38UCSC Ensembl
chr6:106532376..106537175hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216553
Samples
Known GenesPRDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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