A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610522



Internal ID20983593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99273619..99284316hg38UCSC Ensembl
chr7:98871242..98881939hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810698
hg1910698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227486
Samples
Known GenesMYH16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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