A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5964n100



Internal ID20157580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55284590..55378351hg38UCSC Ensembl
chr6:55149388..55243149hg19UCSC Ensembl
chr6:55257347..55351108hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3893762
hg1993762
hg1893762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029279, nsv1015161, nsv1034960, nsv1034005
Samples
Known GenesGFRAL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5964n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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