A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076145



Internal ID21985378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11030..11030hg38UCSC Ensembl
chr9:11030..11030hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076145
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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