A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5995n100



Internal ID22792082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63316957..63392140hg38UCSC Ensembl
chr6:64026862..64102045hg19UCSC Ensembl
chr6:64084821..64160004hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3875184
hg1975184
hg1875184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031548, nsv1030651
Samples
Known GenesLGSN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5995n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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