A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416135



Internal ID21073688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148795962..148804659hg38UCSC Ensembl
chr7:148493054..148501751hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg388698
hg198698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218980
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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