A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221016



Internal ID20788056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39729839..40075751hg38UCSC Ensembl
chr7:39769438..40115350hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38345913
hg19345913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604686
Supporting Variants
Samples
Known GenesCDK13, LINC00265
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221016
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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