A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011180



Internal ID21920523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135548992..135549119hg38UCSC Ensembl
chr9:138440838..138440965hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590873
Samples
Known GenesOBP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011180
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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