A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618945



Internal ID20992016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1198971..1220826hg38UCSC Ensembl
chr7:1238607..1260462hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3821856
hg1921856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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