A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087980



Internal ID21997213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133828356..133828356hg38UCSC Ensembl
chr9:136693478..136693478hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585368
Samples
Known GenesVAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087980
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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