A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv661n54



Internal ID20134085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182809600..182812435hg38UCSC Ensembl
chr1:182778735..182781570hg19UCSC Ensembl
chr1:181045358..181048193hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg382836
hg192836
hg182836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548373, nsv548374
Samples
Known GenesNPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv661n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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