A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228154



Internal ID20795194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149228607..149243449hg38UCSC Ensembl
chr7:148925698..148940540hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3814843
hg1914843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422367
Supporting Variants
Samples
Known GenesZNF212
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228154
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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