A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012860



Internal ID21922203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32965803..32965854hg38UCSC Ensembl
chr7:33005415..33005466hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568178
Samples
Known GenesFKBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012860
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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