A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11297n54



Internal ID19003473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44107701..44114893hg38UCSC Ensembl
chr7:44147300..44154492hg19UCSC Ensembl
chr7:44113825..44121017hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg387193
hg197193
hg187193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606748, nsv606750
Samples
Known GenesAEBP1, MIR4649, POLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11297n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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