A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv793n54



Internal ID22768688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207542754..207568099hg38UCSC Ensembl
chr1:207716099..207741444hg19UCSC Ensembl
chr1:205782722..205808067hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3825346
hg1925346
hg1825346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549087, nsv549088
Samples
Known GenesCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv793n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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