A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1156n209



Internal ID22827231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88832762..89268001hg38UCSC Ensembl
chr2:89132275..89567758hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38435240
hg19435484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5883336, nsv5883706, nsv5869871, nsv5885965, nsv5887519, nsv5874809, nsv5873529, nsv5867791, nsv5881344, nsv5875583, nsv5875447, nsv5887238, nsv5877096, nsv5882816, nsv5875171, nsv5881746, nsv5885476, nsv5881985, nsv5886259, nsv5870054, nsv5887125, nsv5869658, nsv5880720, nsv5868040, nsv5882517, nsv5871646, nsv5884627, nsv5882134, nsv5878897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1156n209
Frequency
Sample Size914
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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