A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753147



Internal ID20529007
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 StatusM
Merged Variants
Supporting Variantsnssv16269409
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753147
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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