A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000833



Internal ID21910176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93311974..93315420hg38UCSC Ensembl
chr6:94021692..94025138hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383447
hg193447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574070
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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