A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7681n223



Internal ID22810649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30197700..30502690hg38UCSC Ensembl
chr9:30197698..30502688hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38304991
hg19304991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6425727, nsv6426280
Samples
Known GenesLOC401497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7681n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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