A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163772



Internal ID21452002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95188001..95188001hg38UCSC Ensembl
chr9:97950283..97950283hg19UCSC 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 Variantsnsv5638265
Supporting Variants
SamplesHG01596
Known GenesFANCC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163772
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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