A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6667n223



Internal ID22809635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53516891..53558882hg38UCSC Ensembl
chr7:53584584..53626575hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3841992
hg1941992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6611646, nsv6609257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6667n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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