A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13005n54



Internal ID20146429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136605258..136696482hg38UCSC Ensembl
chr9:139499710..139590934hg19UCSC Ensembl
chr9:138619531..138710755hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3891225
hg1991225
hg1891225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615980, nsv615977, nsv615979, nsv615975
SamplesNINDS_168, HGDP00512
Known GenesAGPAT2, EGFL7, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13005n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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