A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5977n100



Internal ID19016345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57946158..58032352hg38UCSC Ensembl
chr6:58272436..58358630hg19UCSC Ensembl
chr6:58380395..58466589hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg3886195
hg1986195
hg1886195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032544, nsv1033219, nsv1021741
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5977n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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