A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609359



Internal ID20982430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99027119..99036428hg38UCSC Ensembl
chr7:98624742..98634051hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389310
hg199310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229285
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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