A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014299



Internal ID21923642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99076007..99076077hg38UCSC Ensembl
chr7:98673630..98673700hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564872
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014299
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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