A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225464



Internal ID20792504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3034451..3050025hg38UCSC Ensembl
chr7:3074085..3089659hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3815575
hg1915575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616259
Supporting Variants
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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