A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv177n97



Internal ID22815574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241833619..242147305hg38UCSC Ensembl
chr2:242775796..243089456hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38313687
hg19313661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155933, nsv1155935, nsv1155931, nsv1155932, nsv1155934
Samples
Known GenesCXXC11, LOC728323, PDCD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv177n97
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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