A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12982n54



Internal ID22780877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135571320..135584977hg38UCSC Ensembl
chr9:138463166..138476823hg19UCSC Ensembl
chr9:137602987..137616644hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3813658
hg1913658
hg1813658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615886, nsv615887
SamplesHGDP01179, HGDP00666
Known GenesLOC100130954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12982n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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