A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607220



Internal ID20980291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21872965..21944333hg38UCSC Ensembl
chr7:21912583..21983951hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3871369
hg1971369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224987
Samples
Known GenesCDCA7L, DNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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