A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617651



Internal ID20990722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98546644..98578852hg38UCSC Ensembl
chr7:98175956..98208164hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3832209
hg1932209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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