A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014656



Internal ID21923999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103987698..104201455hg38UCSC Ensembl
chr9:106749979..106963736hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38213758
hg19213758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587855
Samples
Known GenesSMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014656
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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