A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227677



Internal ID20794717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130807865..130808480hg38UCSC Ensembl
chr9:133683252..133683867hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449670
Supporting Variants
Samples
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00049


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