A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11267n54



Internal ID22779162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31550984..31551997hg38UCSC Ensembl
chr7:31590598..31591611hg19UCSC Ensembl
chr7:31557123..31558136hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381014
hg191014
hg181014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606572, nsv606578, nsv606573
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11267n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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