A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n97



Internal ID22815568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87117615..87211079hg38UCSC Ensembl
chr2:87344738..87438202hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3893465
hg1993465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155753, nsv1155762
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv171n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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