A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269409



Internal ID20478627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95188002..95188002hg38UCSC Ensembl
chr9:97950284..97950284hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753147
Supporting Variants
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269409
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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