A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013334



Internal ID21922677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136913442..136914245hg38UCSC Ensembl
chr9:139807894..139808697hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581498
Samples
Known GenesTRAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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