A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226147



Internal ID20793187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91417701..91423300hg38UCSC Ensembl
chr9:94179983..94185582hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436111
Supporting Variants
Samples
Known GenesNFIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


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