A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607870



Internal ID20980941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21565845..21597650hg38UCSC Ensembl
chr7:21605463..21637268hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3831806
hg1931806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235274
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607870
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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