A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437918



Internal ID22495788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75610906..75610992hg38UCSC Ensembl
chr6:76320622..76320708hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902462
Supporting Variants
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437918
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.026


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