A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224895



Internal ID20791935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149142719..149148943hg38UCSC Ensembl
chr7:148839811..148846035hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386225
hg196225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433443
Supporting Variants
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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