A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751250



Internal ID20527110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94686913..94686913hg38UCSC Ensembl
chr9:97449195..97449195hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751250
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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