A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012664



Internal ID21922007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95114154..95114228hg38UCSC Ensembl
chr9:97876436..97876510hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587125
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012664
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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