A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219047



Internal ID20786087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138630673..138643157hg38UCSC Ensembl
chr7:138315418..138327902hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3812485
hg1912485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429480
Supporting Variants
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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