A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075077



Internal ID21984310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99053600..99053600hg38UCSC Ensembl
chr7:98651223..98651223hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562186
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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