A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000788



Internal ID21910131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137832307..137832499hg38UCSC Ensembl
chr9:140726759..140726951hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580928
Samples
Known GenesEHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000788
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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