A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088490



Internal ID21997723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136960449..136960449hg38UCSC Ensembl
chr9:139854901..139854901hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088490
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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