A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223150



Internal ID20790190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12539644..12593555hg38UCSC Ensembl
chr7:12579270..12633180hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3853912
hg1953911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600549
Supporting Variants
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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