A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6658n223



Internal ID22809626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40354032..40469480hg38UCSC Ensembl
chr7:40393631..40509079hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38115449
hg19115449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6605419, nsv6605761
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6658n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer