A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv302n54



Internal ID20133726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61648509..61654909hg38UCSC Ensembl
chr1:62114181..62120581hg19UCSC Ensembl
chr1:61886769..61893169hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg386401
hg196401
hg186401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546402, nsv546393, nsv546392
Samples
Known GenesMGC34796
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv302n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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