A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225191



Internal ID20792231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127414158..127440063hg38UCSC Ensembl
chr9:130176437..130202342hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3825906
hg1925906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443901
Supporting Variants
Samples
Known GenesZNF79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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