A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767653



Internal ID20543513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100100580..100100580hg38UCSC Ensembl
chr9:102862862..102862862hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278051
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767653
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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