A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226765



Internal ID20793805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128392544..128434941hg38UCSC Ensembl
chr7:128032598..128074995hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3842398
hg1942398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415743
Supporting Variants
Samples
Known GenesIMPDH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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