A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12749n54



Internal ID22780644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71140518..71153632hg38UCSC Ensembl
chr9:73755434..73768548hg19UCSC Ensembl
chr9:72945254..72958368hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3813115
hg1913115
hg1813115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614602, nsv614604, nsv614601, nsv614600, nsv614599, nsv614603
SamplesNINDS_174
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12749n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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