A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220362



Internal ID20787402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107555601..107584900hg38UCSC Ensembl
chr7:107196046..107225345hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3829300
hg1929300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615847
Supporting Variants
Samples
Known GenesBCAP29, COG5, DUS4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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