A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11354n54



Internal ID19003530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57091428..57549195hg38UCSC Ensembl
chr7:57159135..57608901hg19UCSC Ensembl
chr7:57163077..57612843hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38457768
hg19449767
hg18449767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607050, nsv607046, nsv607049, nsv607047
Samples1798860210_A
Known GenesGUSBP10, MIR3147, ZNF479, ZNF716
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11354n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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