A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227319



Internal ID20794359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20774301..20803600hg38UCSC Ensembl
chr7:20813921..20843219hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3829300
hg1929299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601848
Supporting Variants
Samples
Known GenesSP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227319
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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