A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602708



Internal ID20975779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155075670..155761341hg38UCSC Ensembl
chr6:155396804..156082475hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38685672
hg19685672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216680
Samples
Known GenesCLDN20, NOX3, TFB1M, TIAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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