A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7932n223



Internal ID22810900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123912601..123919700hg38UCSC Ensembl
chr9:126674880..126681979hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6437829, nsv6447899
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7932n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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