A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10642n54



Internal ID22778537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45562734..45578238hg38UCSC Ensembl
chr6:45530471..45545975hg19UCSC Ensembl
chr6:45638449..45653953hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3815505
hg1915505
hg1815505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603009, nsv603010
Samples1780862378_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10642n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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