A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2n97



Internal ID22815399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1575421..1756148hg38UCSC Ensembl
chr1:1510801..1687587hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38180728
hg19176787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155131, nsv1156357
Samples
Known GenesC1orf233, CDK11A, CDK11B, MIB2, MMP23A, MMP23B, NADK, SLC35E2, SLC35E2B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv2n97
Frequency
Sample Size131
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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