A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6689n223



Internal ID22809657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57722537..57976360hg38UCSC Ensembl
chr7:57782243..58036066hg19UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38253824
hg19253824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6609499, nsv6611337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6689n223
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