A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608451



Internal ID20981522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40847307..40936595hg38UCSC Ensembl
chr7:40886906..40976194hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3889289
hg1989289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224055
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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