A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236145



Internal ID20803185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15561578..15599963hg38UCSC Ensembl
chr7:15601203..15639588hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3838386
hg1938386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604498
Supporting Variants
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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