A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4930n100



Internal ID22791017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158557789..158588105hg38UCSC Ensembl
chr3:158275578..158305894hg19UCSC Ensembl
chr3:159758272..159788588hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3830317
hg1930317
hg1830317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013242, nsv1001944, nsv1013112
Samples
Known GenesLOC100996447, MLF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4930n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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