A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4677n100



Internal ID20156293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8469180..8507979hg38UCSC Ensembl
chr3:8510866..8549665hg19UCSC Ensembl
chr3:8485866..8524665hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3838800
hg1938800
hg1838800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998459, nsv1014154
Samples
Known GenesLMCD1, LMCD1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4677n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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