A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100137



Internal ID22009370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136897819..136897819hg38UCSC Ensembl
chr9:139792271..139792271hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583778
Samples
Known GenesTRAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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